A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576946



Internal ID18875227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:8518409..8552852hg38UCSC Ensembl
Innerchr2:8658539..8692982hg19UCSC Ensembl
Innerchr2:8575990..8610433hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3834444
hg1934444
hg1834444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011736
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)nssv3576946
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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