A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528646



Internal ID15109253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:122048207..122062539hg38UCSC Ensembl
Innerchr3:121767054..121781386hg19UCSC Ensembl
Innerchr3:123249744..123264076hg18UCSC Ensembl
Innerchr3:123249744..123264076hg17UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3814333
hg1914333
hg1814333
hg1714333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705278
Samples
Known GenesCD86
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528646
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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