A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615047



Internal ID16402456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103358388..103444989hg38UCSC Ensembl
Innerchr9:106120670..106207271hg19UCSC Ensembl
Innerchr9:105160491..105247092hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3886602
hg1986602
hg1886602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140624
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615047
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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