A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575692



Internal ID16363101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:56074499..56094916hg38UCSC Ensembl
Innerchr17:54151860..54172277hg19UCSC Ensembl
Innerchr17:51506859..51527276hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3820418
hg1920418
hg1820418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5713n54
Supporting Variantsnssv874125
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575692
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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