A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv849607



Internal ID15796877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98648030..98650363hg38UCSC Ensembl
Innerchr15:99191259..99193592hg19UCSC Ensembl
Innerchr15:97008782..97011115hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382334
hg192334
hg182334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570704
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)nssv849607
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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