A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875748



Internal ID16169704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62978029..63174891hg38UCSC Ensembl
Innerchr17:61055390..61252252hg19UCSC Ensembl
Innerchr17:58409122..58605984hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38196863
hg19196863
hg18196863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575850
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)nssv875748
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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