A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570506



Internal ID16357915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93191753..93253049hg38UCSC Ensembl
Innerchr15:93734982..93796278hg19UCSC Ensembl
Innerchr15:91535986..91597282hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3861297
hg1961297
hg1861297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149609
SamplesNINDS_219
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570506
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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