A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149606



Internal ID15530154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92573289..92590195hg38UCSC Ensembl
Innerchr15:93116519..93133425hg19UCSC Ensembl
Innerchr15:90917523..90934429hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3816907
hg1916907
hg1816907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570503
Supporting Variants
SamplesHGDP00902
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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