A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv467537



Internal ID15035601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6146375..6146628hg38UCSC Ensembl
Outerchr10:6141842..6147399hg38UCSC Ensembl
Innerchr10:6188338..6188591hg19UCSC Ensembl
Outerchr10:6183805..6189362hg19UCSC Ensembl
Innerchr10:6228344..6228597hg18UCSC Ensembl
Outerchr10:6223811..6229368hg18UCSC Ensembl
Innerchr10:6192344..6192597hg16UCSC Ensembl
Outerchr10:6187811..6193368hg16UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg385558
hg195558
hg185558
hg165558
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele OriginGermline
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv437656
Supporting Variants
SamplesNA19211
Known GenesPFKFB3
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nssv467537
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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