A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614165



Internal ID16401574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35605153..35605921hg38UCSC Ensembl
Innerchr9:35605150..35605918hg19UCSC Ensembl
Innerchr9:35595150..35595918hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38769
hg19769
hg18769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132860, nssv1132858, nssv1132859
Samples
Known GenesTESK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614165
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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