A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604975



Internal ID16392384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:154910548..154950818hg38UCSC Ensembl
Innerchr6:155231682..155271952hg19UCSC Ensembl
Innerchr6:155273374..155313644hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3840271
hg1940271
hg1840271
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155099
SamplesHGDP01034
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604975
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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