A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149245



Internal ID15873041
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 StatusS
Merged Variantsnsv570241
Supporting Variants
SamplesHGDP00105
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149245
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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