A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573904



Internal ID16361313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:178833..181104hg38UCSC Ensembl
Innerchr17:28624..30895hg19UCSC Ensembl
Innerchr17:28624..30895hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg382272
hg192272
hg182272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv864207
Samples
Known GenesDOC2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573904
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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