A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014685



Internal ID19103902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35593856..35863564hg38UCSC Ensembl
Innerchr2:35818922..36088630hg19UCSC Ensembl
Innerchr2:35672426..35942134hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38269709
hg19269709
hg18269709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3788n100
Supporting Variantsnssv3581243, nssv3725960
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)nsv1014685
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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