A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3581465



Internal ID18879746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35873895..35907877hg38UCSC Ensembl
Innerchr2:36098961..36132943hg19UCSC Ensembl
Innerchr2:35952465..35986447hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3833983
hg1933983
hg1833983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013428
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)nssv3581465
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