A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517858



Internal ID15445151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:145144438..145148502hg38UCSC Ensembl
Innerchr7:144841531..144845595hg19UCSC Ensembl
Innerchr7:144472464..144476528hg18UCSC Ensembl
Innerchr7:144279179..144283243hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg384065
hg194065
hg184065
hg174065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv433n21
Supporting Variantsnssv695262
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517858
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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