A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582159



Internal ID18880440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:82245787..82378964hg38UCSC Ensembl
Innerchr2:82472911..82606088hg19UCSC Ensembl
Innerchr2:82326422..82459599hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38133178
hg19133178
hg18133178
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007519
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)nssv3582159
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