A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603237



Internal ID16043960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57904941..58453777hg38UCSC Ensembl
Innerchr6:58231219..58780055hg19UCSC Ensembl
Innerchr6:58339178..58888014hg18UCSC Ensembl
Cytoband6p11.1
Allele length
AssemblyAllele length
hg38548837
hg19548837
hg18548837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10686n54
Supporting Variantsnssv1061045
Samples
Known GenesGUSBP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603237
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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