A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074581



Internal ID15581081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152069377..152070695hg38UCSC Ensembl
Innerchr6:152390512..152391830hg19UCSC Ensembl
Innerchr6:152432205..152433523hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381319
hg191319
hg181319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604905
Supporting Variants
Samples
Known GenesESR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1074581
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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