A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574320



Internal ID16015043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6855195..6957288hg38UCSC Ensembl
Innerchr17:6758514..6860607hg19UCSC Ensembl
Innerchr17:6699238..6801331hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38102094
hg19102094
hg18102094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5440n54
Supporting Variantsnssv866670, nssv866669
Samples
Known GenesALOX12P2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574320
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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