A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576128



Internal ID16363537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:79936326..79938459hg38UCSC Ensembl
Innerchr17:77910125..77912258hg19UCSC Ensembl
Innerchr17:75524720..75526853hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382134
hg192134
hg182134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv876896
Samples
Known GenesTBC1D16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576128
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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