A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570241



Internal ID16357650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82069784..82104006hg38UCSC Ensembl
Innerchr15:82362125..82396347hg19UCSC Ensembl
Innerchr15:80149180..80183402hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3834223
hg1934223
hg1834223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149245
SamplesHGDP00105
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570241
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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