A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517402



Internal ID15444695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:136667463..136678816hg38UCSC Ensembl
Innerchr5:136003152..136014505hg19UCSC Ensembl
Innerchr5:136031051..136042404hg18UCSC Ensembl
Innerchr5:136031051..136042404hg17UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3811354
hg1911354
hg1811354
hg1711354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692760, nssv664206, nssv685780, nssv656044, nssv684282, nssv682302, nssv668737, nssv679506, nssv651916, nssv656368, nssv677328, nssv669811, nssv660458, nssv661546, nssv662775, nssv665179, nssv679477, nssv685737, nssv662154, nssv671094, nssv664857
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517402
Frequency
Sample Size2026
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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