A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700383



Internal ID15437035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87547223..87551142hg38UCSC Ensembl
Innerchr16:87580829..87584748hg19UCSC Ensembl
Innerchr16:86138330..86142249hg18UCSC Ensembl
Innerchr16:86138330..86142249hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383920
hg193920
hg183920
hg173920
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524450
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700383
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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