A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064059



Internal ID18806590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:63271412..63453079hg38UCSC Ensembl
Innerchr17:61348773..61530440hg19UCSC Ensembl
Innerchr17:58702505..58884172hg18UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38181668
hg19181668
hg18181668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567723
Samples
Known GenesCYB561, TANC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064059
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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