A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570662



Internal ID16358071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98258496..98260387hg38UCSC Ensembl
Innerchr15:98801725..98803616hg19UCSC Ensembl
Innerchr15:96619248..96621139hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381892
hg191892
hg181892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv849398
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570662
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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