A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580119



Internal ID18531714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:107924531..108715172hg38UCSC Ensembl
Innerchr2:108540987..109331628hg19UCSC Ensembl
Innerchr2:107907419..108698060hg18UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg38790642
hg19790642
hg18790642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005474
Supporting Variants
Samples
Known GenesGCC2, LIMS1, SLC5A7, SULT1C2, SULT1C2P1, SULT1C3, SULT1C4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580119
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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