A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066998



Internal ID18809529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69063897..69094334hg38UCSC Ensembl
Innerchr17:67060038..67090475hg19UCSC Ensembl
Innerchr17:64571633..64602070hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3830438
hg1930438
hg1830438
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567759
Samples
Known GenesABCA6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066998
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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