A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527772



Internal ID15455065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140010959..140016306hg38UCSC Ensembl
Innerchr6:140332096..140337443hg19UCSC Ensembl
Innerchr6:140373789..140379136hg18UCSC Ensembl
Innerchr6:140373789..140379136hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg385348
hg195348
hg185348
hg175348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704261
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527772
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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