A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437552



Internal ID15382858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79179852..79197820hg38UCSC Ensembl
Outerchr7:79172593..79227388hg38UCSC Ensembl
Innerchr7:78809168..78827136hg19UCSC Ensembl
Outerchr7:78801909..78856704hg19UCSC Ensembl
Innerchr7:78647104..78665072hg18UCSC Ensembl
Outerchr7:78639845..78694640hg18UCSC Ensembl
Innerchr7:78421219..78439187hg16UCSC Ensembl
Outerchr7:78413960..78468755hg16UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3854796
hg1954796
hg1854796
hg1654796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv131n17
Supporting Variantsnssv467433
SamplesNA18872
Known GenesMAGI2
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)nsv437552
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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