A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527797



Internal ID15108404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57952620..58042353hg38UCSC Ensembl
Innerchr6:58278898..58368631hg19UCSC Ensembl
Innerchr6:58386857..58476590hg18UCSC Ensembl
Innerchr6:58386857..58476590hg17UCSC Ensembl
Cytoband6p11.1
Allele length
AssemblyAllele length
hg3889734
hg1989734
hg1889734
hg1789734
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704289
Samples
Known GenesGUSBP4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527797
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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