A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660623



Internal ID15050589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11433733..11479757hg38UCSC Ensembl
Innerchr16:11527589..11573613hg19UCSC Ensembl
Innerchr16:11435090..11481114hg18UCSC Ensembl
Innerchr16:11435090..11481114hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3846025
hg1946025
hg1846025
hg1746025
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520088
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660623
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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