A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066968



Internal ID18809499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:64215762..64332226hg38UCSC Ensembl
Innerchr17:62293122..62409586hg19UCSC Ensembl
Innerchr17:59646854..59763318hg18UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38116465
hg19116465
hg18116465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567725
Samples
Known GenesPECAM1, TEX2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066968
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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