A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510234



Internal ID20883551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84211283..84311387hg38UCSC Ensembl
chr16:84244889..84344993hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38100105
hg19100105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032966
Samples
Known GenesKCNG4, WFDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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