A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv849606



Internal ID16143562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98648030..98649896hg38UCSC Ensembl
Innerchr15:99191259..99193125hg19UCSC Ensembl
Innerchr15:97008782..97010648hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381867
hg191867
hg181867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570703
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)nssv849606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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