A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155796



Internal ID15876223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150515540..150552630hg38UCSC Ensembl
Innerchr6:150836676..150873766hg19UCSC Ensembl
Innerchr6:150878369..150915459hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3837091
hg1937091
hg1837091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604850
Supporting Variants
SamplesHGDP00805
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155796
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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