A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573903



Internal ID16014626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:171764..181795hg38UCSC Ensembl
Innerchr17:21555..31586hg19UCSC Ensembl
Innerchr17:21555..31586hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3810032
hg1910032
hg1810032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5346n54
Supporting Variantsnssv864206
Samples
Known GenesDOC2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573903
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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