A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv849598



Internal ID15796868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98647653..98650363hg38UCSC Ensembl
Innerchr15:99190882..99193592hg19UCSC Ensembl
Innerchr15:97008405..97011115hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382711
hg192711
hg182711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570697
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)nssv849598
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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