A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613257



Internal ID16400666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7015330..7037370hg38UCSC Ensembl
Innerchr9:7015330..7037370hg19UCSC Ensembl
Innerchr9:7005330..7027370hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3822041
hg1922041
hg1822041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126848
Samples
Known GenesKDM4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613257
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