A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520330



Internal ID15447623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:120110981..120163454hg38UCSC Ensembl
Innerchr6:120432127..120484600hg19UCSC Ensembl
Innerchr6:120473826..120526299hg18UCSC Ensembl
Innerchr6:120473826..120526299hg17UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3852474
hg1952474
hg1852474
hg1752474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697352
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520330
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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