A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582011



Internal ID18880292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76317328..76359573hg38UCSC Ensembl
Innerchr2:76544454..76586699hg19UCSC Ensembl
Innerchr2:76397962..76440207hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3842246
hg1942246
hg1842246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003728
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)nssv3582011
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