A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517755



Internal ID15445048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9454787..9479634hg38UCSC Ensembl
Innerchr1:9514846..9539693hg19UCSC Ensembl
Innerchr1:9437433..9462280hg18UCSC Ensembl
Innerchr1:9449112..9473959hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3824848
hg1924848
hg1824848
hg1724848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692200, nssv661666, nssv674995, nssv693425, nssv670279, nssv658552, nssv653129
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517755
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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