A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv849601



Internal ID16143557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98647653..98650539hg38UCSC Ensembl
Innerchr15:99190882..99193768hg19UCSC Ensembl
Innerchr15:97008405..97011291hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382887
hg192887
hg182887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570698
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)nssv849601
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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