A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517277



Internal ID15444570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:107317624..107324829hg38UCSC Ensembl
Innerchr5:106653325..106660530hg19UCSC Ensembl
Innerchr5:106681224..106688429hg18UCSC Ensembl
Innerchr5:106681224..106688429hg17UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg387206
hg197206
hg187206
hg177206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654189, nssv693964
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517277
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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