A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575716



Internal ID16363125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:56701259..56729478hg38UCSC Ensembl
Innerchr17:54778620..54806839hg19UCSC Ensembl
Innerchr17:52133619..52161838hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3828220
hg1928220
hg1828220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv874248
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575716
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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