A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998133



Internal ID19157670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34434857..34511978hg38UCSC Ensembl
Innerchr2:34659924..34737045hg19UCSC Ensembl
Innerchr2:34513428..34590549hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3877122
hg1977122
hg1877122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3758n100
Supporting Variantsnssv3580960, nssv3580964, nssv3580957, nssv3728032, nssv3728029, nssv3580958, nssv3728028, nssv3728035, nssv3728026, nssv3728027, nssv3728034, nssv3728033, nssv3580961, nssv3728030, nssv3580959, nssv3728036, nssv3728031, nssv3580963, nssv3580962
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)nsv998133
Frequency
Sample Size11257
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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