A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv874068



Internal ID16168024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54114301..54220259hg38UCSC Ensembl
Innerchr17:52191662..52297620hg19UCSC Ensembl
Innerchr17:49546661..49652619hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38105959
hg19105959
hg18105959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575651
Supporting Variants
Samples
Known GenesMIR548AJ2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv874068
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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