A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521576



Internal ID15448869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:115107468..115279505hg38UCSC Ensembl
Innerchr6:115428632..115600669hg19UCSC Ensembl
Innerchr6:115535325..115707362hg18UCSC Ensembl
Innerchr6:115535325..115707362hg17UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38172038
hg19172038
hg18172038
hg17172038
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698192
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521576
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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