A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703518



Internal ID15440170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:42027559..42030188hg38UCSC Ensembl
Innerchr6:41995297..41997926hg19UCSC Ensembl
Innerchr6:42103275..42105904hg18UCSC Ensembl
Innerchr6:42103275..42105904hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg382630
hg192630
hg182630
hg172630
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527131
Supporting Variants
Samples
Known GenesCCND3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703518
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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