A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576093



Internal ID16363502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77833684..77862451hg38UCSC Ensembl
Innerchr17:75829766..75858533hg19UCSC Ensembl
Innerchr17:73341361..73370128hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3828768
hg1928768
hg1828768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv876248
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576093
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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