A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655246



Internal ID15045212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10879763..10887018hg38UCSC Ensembl
Innerchr6:10879996..10887251hg19UCSC Ensembl
Innerchr6:10987982..10995237hg18UCSC Ensembl
Innerchr6:10987982..10995237hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg387256
hg197256
hg187256
hg177256
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519302
Supporting Variants
Samples
Known GenesGCM2, SYCP2L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655246
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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