A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437689



Internal ID15382995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78350669..78351149hg38UCSC Ensembl
Outerchr10:78344884..78354408hg38UCSC Ensembl
Innerchr10:80110426..80110906hg19UCSC Ensembl
Outerchr10:80104641..80114165hg19UCSC Ensembl
Innerchr10:79780432..79780912hg18UCSC Ensembl
Outerchr10:79774647..79784171hg18UCSC Ensembl
Innerchr10:79455029..79455509hg16UCSC Ensembl
Outerchr10:79449244..79458768hg16UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg389525
hg199525
hg189525
hg169525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467570
SamplesNA19208
Known Genes
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)nsv437689
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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