A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065602



Internal ID19154821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52609623..52763926hg38UCSC Ensembl
Innerchr17:50686983..50841286hg19UCSC Ensembl
Innerchr17:48041982..48196285hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38154304
hg19154304
hg18154304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568612
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065602
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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