A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521503



Internal ID15448796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:159792330..159825688hg38UCSC Ensembl
Innerchr1:159762120..159795478hg19UCSC Ensembl
Innerchr1:158028744..158062102hg18UCSC Ensembl
Innerchr1:156575193..156608551hg17UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3833359
hg1933359
hg1833359
hg1733359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698120
Samples
Known GenesFCRL6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521503
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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