A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705547



Internal ID15442199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8913275..8953502hg38UCSC Ensembl
Innerchr3:8954959..8995186hg19UCSC Ensembl
Innerchr3:8929959..8970186hg18UCSC Ensembl
Innerchr3:8929959..8970186hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3840228
hg1940228
hg1840228
hg1740228
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528867
Supporting Variants
Samples
Known GenesRAD18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705547
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