A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061151



Internal ID18803682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68885476..68977776hg38UCSC Ensembl
Innerchr17:66881617..66973917hg19UCSC Ensembl
Innerchr17:64393212..64485512hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3892301
hg1992301
hg1892301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567757
Samples
Known GenesABCA8, ABCA9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061151
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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