A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596275



Internal ID18894556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:86624023..86676563hg38UCSC Ensembl
Innerchr3:86673173..86725713hg19UCSC Ensembl
Innerchr3:86755863..86808403hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3852541
hg1952541
hg1852541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009339
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3596275
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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