A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3499893



Internal ID19087534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208908917..208950507hg38UCSC Ensembl
Innerchr1:209082262..209123852hg19UCSC Ensembl
Innerchr1:207148885..207190475hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3841591
hg1941591
hg1841591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999126
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)nssv3499893
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