A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527103



Internal ID15454396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7356865..7367510hg38UCSC Ensembl
Innerchr5:7356978..7367623hg19UCSC Ensembl
Innerchr5:7409978..7420623hg18UCSC Ensembl
Innerchr5:7409978..7420623hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3810646
hg1910646
hg1810646
hg1710646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703483
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527103
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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