A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156222



Internal ID15875627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6672097..6731786hg38UCSC Ensembl
Innerchr9:6672097..6731786hg19UCSC Ensembl
Innerchr9:6662097..6721786hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3859690
hg1959690
hg1859690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613213
Supporting Variants
SamplesHGDP00711
Known GenesKDM4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156222
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer