A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699705



Internal ID15436357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:94307465..94453604hg38UCSC Ensembl
Innerchr5:93643170..93789309hg19UCSC Ensembl
Innerchr5:93668926..93815065hg18UCSC Ensembl
Innerchr5:93668926..93815065hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38146140
hg19146140
hg18146140
hg17146140
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523867
Supporting Variants
Samples
Known GenesKIAA0825
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699705
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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