A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521296



Internal ID15101903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151835062..151835442hg38UCSC Ensembl
Innerchr6:152156197..152156577hg19UCSC Ensembl
Innerchr6:152197890..152198270hg18UCSC Ensembl
Innerchr6:152248311..152248691hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38381
hg19381
hg18381
hg17381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697902
Samples
Known GenesESR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521296
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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