A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690764



Internal ID15427416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:37021376..37021811hg38UCSC Ensembl
Innerchr6:36989152..36989587hg19UCSC Ensembl
Innerchr6:37097130..37097565hg18UCSC Ensembl
Innerchr6:37097130..37097565hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38436
hg19436
hg18436
hg17436
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515488
Supporting Variants
Samples
Known GenesFGD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690764
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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