A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705263



Internal ID15441915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91891918..92490915hg38UCSC Ensembl
Innerchr6:92601636..93200633hg19UCSC Ensembl
Innerchr6:92658357..93257354hg18UCSC Ensembl
Innerchr6:92658357..93257354hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38598998
hg19598998
hg18598998
hg17598998
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528633
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705263
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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