A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524314



Internal ID15451607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:6786234..6991071hg38UCSC Ensembl
Innerchr6:6786467..6991304hg19UCSC Ensembl
Innerchr6:6731466..6936303hg18UCSC Ensembl
Innerchr6:6731466..6936303hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38204838
hg19204838
hg18204838
hg17204838
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700216
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524314
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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