A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690212



Internal ID15080178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70714505..70714794hg38UCSC Ensembl
Innerchr16:70748408..70748697hg19UCSC Ensembl
Innerchr16:69305909..69306198hg18UCSC Ensembl
Innerchr16:69305909..69306198hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38290
hg19290
hg18290
hg17290
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517391
Supporting Variants
Samples
Known GenesVAC14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690212
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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