A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604890



Internal ID16045613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151771614..151797984hg38UCSC Ensembl
Innerchr6:152092749..152119119hg19UCSC Ensembl
Innerchr6:152134442..152160812hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3826371
hg1926371
hg1826371
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1074464
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604890
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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