A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573886



Internal ID16014609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:170860..181706hg38UCSC Ensembl
Innerchr17:20651..31497hg19UCSC Ensembl
Innerchr17:20651..31497hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3810847
hg1910847
hg1810847
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5347n54
Supporting Variantsnssv864164, nssv864166, nssv864165
Samples
Known GenesDOC2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573886
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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