A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv849604



Internal ID15796874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98647822..98652883hg38UCSC Ensembl
Innerchr15:99191051..99196112hg19UCSC Ensembl
Innerchr15:97008574..97013635hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg385062
hg195062
hg185062
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570701
Supporting Variants
Samples
Known GenesIGF1R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv849604
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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