A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574442



Internal ID16361851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15280310..15281400hg38UCSC Ensembl
Innerchr17:15183627..15184717hg19UCSC Ensembl
Innerchr17:15124352..15125442hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381091
hg191091
hg181091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5464n54
Supporting Variantsnssv868368, nssv868369, nssv868370, nssv868367, nssv868373, nssv868371, nssv868372
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574442
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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