A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698884



Internal ID15088850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81724858..81744886hg38UCSC Ensembl
Innerchr16:81758463..81778491hg19UCSC Ensembl
Innerchr16:80315964..80335992hg18UCSC Ensembl
Innerchr16:80315964..80335992hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3820029
hg1920029
hg1820029
hg1720029
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523172
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698884
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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