A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726004



Internal ID19024285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:47975022..48135499hg38UCSC Ensembl
Innerchr2:48202161..48362638hg19UCSC Ensembl
Innerchr2:48055665..48216142hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38160478
hg19160478
hg18160478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000455
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)nssv3726004
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