A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002915



Internal ID19092132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34697936..34827041hg38UCSC Ensembl
Innerchr2:34923003..35052108hg19UCSC Ensembl
Innerchr2:34776507..34905612hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38129106
hg19129106
hg18129106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3782n100
Supporting Variantsnssv3581122
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)nsv1002915
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