A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519302



Internal ID15099909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10879763..10892266hg38UCSC Ensembl
Innerchr6:10879996..10892499hg19UCSC Ensembl
Innerchr6:10987982..11000485hg18UCSC Ensembl
Innerchr6:10987982..11000485hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3812504
hg1912504
hg1812504
hg1712504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672641, nssv655246
Samples
Known GenesGCM2, SYCP2L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519302
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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