A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574170



Internal ID16361579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1052635..1053169hg38UCSC Ensembl
Innerchr17:955875..956409hg19UCSC Ensembl
Innerchr17:902625..903159hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38535
hg19535
hg18535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5412n54
Supporting Variantsnssv866339
Samples
Known GenesABR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574170
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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