A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518964



Internal ID15099571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179766597..179800286hg38UCSC Ensembl
Innerchr5:179193598..179227286hg19UCSC Ensembl
Innerchr5:179126204..179159892hg18UCSC Ensembl
Innerchr5:179126204..179159892hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3833690
hg1933689
hg1833689
hg1733689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696431
Samples
Known GenesLTC4S, MAML1, MGAT4B, MIR1229
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518964
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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