A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176083



Internal ID15508133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69485135..69504046hg38UCSC Ensembl
Innerchr9:72100051..72118962hg19UCSC Ensembl
Innerchr9:71289871..71308782hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3818912
hg1918912
hg1818912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614572
Supporting Variants
Samples1780862345_A
Known GenesAPBA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176083
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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