A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613258



Internal ID16400667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7030268..7084558hg38UCSC Ensembl
Innerchr9:7030268..7084558hg19UCSC Ensembl
Innerchr9:7020268..7074558hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3854291
hg1954291
hg1854291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156225
Samples1780862573_A
Known GenesKDM4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613258
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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