A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615917



Internal ID16056640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135689825..135724212hg38UCSC Ensembl
Innerchr9:138581671..138616058hg19UCSC Ensembl
Innerchr9:137721492..137755879hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3834388
hg1934388
hg1834388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12992n54
Supporting Variantsnssv1148248
Samples
Known GenesKCNT1, SOHLH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615917
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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