A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579814



Internal ID18878095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89896137..90205353hg38UCSC Ensembl
Innerchr2:89934947..90244220hg19UCSC Ensembl
Innerchr2:89571989..89881525hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38309217
hg19309274
hg18309537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013040
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)nssv3579814
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