A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580577



Internal ID18878858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89956215..90282526hg38UCSC Ensembl
Innerchr2:89995025..90321385hg19UCSC Ensembl
Innerchr2:89632330..89958690hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38326312
hg19326361
hg18326361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013815
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)nssv3580577
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