A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695008



Internal ID15084974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10482629..10542543hg38UCSC Ensembl
Innerchr6:10482862..10542776hg19UCSC Ensembl
Innerchr6:10590848..10650762hg18UCSC Ensembl
Innerchr6:10590848..10650762hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3859915
hg1959915
hg1859915
hg1759915
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522231
Supporting Variants
Samples
Known GenesGCNT2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695008
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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