A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061687



Internal ID18804218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46267481..46358076hg38UCSC Ensembl
Innerchr17:44344847..44435442hg19UCSC Ensembl
Innerchr17:41700624..41791184hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3890596
hg1990596
hg1890561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564234
Samples
Known GenesARL17A, ARL17B, LRRC37A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061687
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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