A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604892



Internal ID16045615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152068833..152070798hg38UCSC Ensembl
Innerchr6:152389968..152391933hg19UCSC Ensembl
Innerchr6:152431661..152433626hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381966
hg191966
hg181966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10970n54
Supporting Variantsnssv1074466
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604892
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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