A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066746



Internal ID19155965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:71190740..71263171hg38UCSC Ensembl
Innerchr17:69186881..69259312hg19UCSC Ensembl
Innerchr17:66698476..66770907hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3872432
hg1972432
hg1872432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3279n100
Supporting Variantsnssv3567768
Samples
Known GenesCASC17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066746
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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