A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061987



Internal ID19151206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15906703..15951821hg38UCSC Ensembl
Innerchr17:15810017..15855135hg19UCSC Ensembl
Innerchr17:15750742..15795860hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3845119
hg1945119
hg1845119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560423
Samples
Known GenesADORA2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061987
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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