A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580862



Internal ID18532457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:131290833..131612296hg38UCSC Ensembl
Innerchr2:132048406..132369869hg19UCSC Ensembl
Innerchr2:131764876..132086339hg18UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38321464
hg19321464
hg18321464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014682
Supporting Variants
Samples
Known GenesCCDC74A, LINC01120, LOC150776, LOC401010, LOC440910, MIR4784, MZT2A, POTEKP, RNU6-81P, TUBA3D, WTH3DI
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580862
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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