A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615254



Internal ID16402663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116500349..116577184hg38UCSC Ensembl
Innerchr9:119262628..119339463hg19UCSC Ensembl
Innerchr9:118302449..118379284hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3876836
hg1976836
hg1876836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141283
Samples
Known GenesASTN2, LOC100128505
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615254
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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