A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875749



Internal ID16169705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62978029..63280171hg38UCSC Ensembl
Innerchr17:61055390..61357532hg19UCSC Ensembl
Innerchr17:58409122..58711264hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38302143
hg19302143
hg18302143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575851
Supporting Variants
Samples
Known GenesMIR548W, TANC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875749
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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