A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574171



Internal ID16361580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1052635..1053277hg38UCSC Ensembl
Innerchr17:955875..956517hg19UCSC Ensembl
Innerchr17:902625..903267hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38643
hg19643
hg18643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5412n54
Supporting Variantsnssv866340
Samples
Known GenesABR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574171
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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