A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603238



Internal ID16043961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57946345..58031416hg38UCSC Ensembl
Innerchr6:58272623..58357694hg19UCSC Ensembl
Innerchr6:58380582..58465653hg18UCSC Ensembl
Cytoband6p11.1
Allele length
AssemblyAllele length
hg3885072
hg1985072
hg1885072
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154092
SamplesHGDP00939
Known GenesGUSBP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603238
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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