A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3724976



Internal ID19023257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:51418866..51479546hg38UCSC Ensembl
Innerchr17:49496227..49556907hg19UCSC Ensembl
Innerchr17:46851226..46911906hg18UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3860681
hg1960681
hg1860681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055993
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)nssv3724976
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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