A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155782



Internal ID15508079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:134365722..134423074hg38UCSC Ensembl
Innerchr6:134686860..134744212hg19UCSC Ensembl
Innerchr6:134728553..134785905hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3857353
hg1957353
hg1857353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604721
Supporting Variants
Samples1780862310_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155782
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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