A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591564



Internal ID16378973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:127104495..127145561hg38UCSC Ensembl
Innerchr3:126823338..126864404hg19UCSC Ensembl
Innerchr3:128306028..128347094hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3841067
hg1941067
hg1841067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv972921
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591564
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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