A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520206



Internal ID15447499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:165934725..165944537hg38UCSC Ensembl
Innerchr1:165903962..165913774hg19UCSC Ensembl
Innerchr1:164170586..164180398hg18UCSC Ensembl
Innerchr1:162635620..162645432hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg389813
hg199813
hg189813
hg179813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692343, nssv698363, nssv704968, nssv661788
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520206
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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