A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067384



Internal ID19156603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:26943373..27286596hg38UCSC Ensembl
Innerchr17:25270399..25613622hg19UCSC Ensembl
Innerchr17:22294526..22637749hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg38343224
hg19343224
hg18343224
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3135n100
Supporting Variantsnssv3561032
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)nsv1067384
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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