A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615297



Internal ID16402706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125746314..125747877hg38UCSC Ensembl
Innerchr9:128508593..128510156hg19UCSC Ensembl
Innerchr9:127548414..127549977hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381564
hg191564
hg181564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12867n54
Supporting Variantsnssv1141324, nssv1141322, nssv1141323
Samples
Known GenesPBX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615297
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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