A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3725151



Internal ID19023432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:70424827..70510729hg38UCSC Ensembl
Innerchr17:68420968..68506870hg19UCSC Ensembl
Innerchr17:65932563..66018465hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3885903
hg1985903
hg1885903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059003
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)nssv3725151
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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