A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500963



Internal ID20874193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21234291..21237787hg38UCSC Ensembl
chr16:21245612..21249108hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg383497
hg193497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028839
Samples
Known GenesANKS4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500963
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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