A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570640



Internal ID16358049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97666007..97705293hg38UCSC Ensembl
Innerchr15:98209237..98248523hg19UCSC Ensembl
Innerchr15:96010241..96049527hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3839287
hg1939287
hg1839287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149165
SamplesHGDP00956
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570640
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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