A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579151



Internal ID18877432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:31664865..31797526hg38UCSC Ensembl
Innerchr2:31889934..32022595hg19UCSC Ensembl
Innerchr2:31743438..31876099hg18UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg38132662
hg19132662
hg18132662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003376
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)nssv3579151
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