A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037264



Internal ID18779795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:98841680..98882395hg38UCSC Ensembl
Innerchr15:99384909..99425624hg19UCSC Ensembl
Innerchr15:97202432..97243147hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3840716
hg1940716
hg1840716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718219
Samples
Known GenesIGF1R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037264
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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