A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518755



Internal ID15099362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6878131..6942063hg38UCSC Ensembl
Innerchr3:6919818..6983750hg19UCSC Ensembl
Innerchr3:6894818..6958750hg18UCSC Ensembl
Innerchr3:6894818..6958750hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3863933
hg1963933
hg1863933
hg1763933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696203
Samples
Known GenesGRM7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518755
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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