A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568607



Internal ID18866888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:50907598..50950216hg38UCSC Ensembl
Innerchr17:48984959..49027577hg19UCSC Ensembl
Innerchr17:46339958..46382576hg18UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3842619
hg1942619
hg1842619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057889
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)nssv3568607
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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