A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063597



Internal ID19152816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77166882..77188461hg38UCSC Ensembl
Innerchr17:75162964..75184543hg19UCSC Ensembl
Innerchr17:72674559..72696138hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3821580
hg1921580
hg1821580
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567814
Samples
Known GenesSEC14L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063597
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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