A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498678



Internal ID20871891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82022629..82027721hg38UCSC Ensembl
chr16:82056234..82061326hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg385093
hg195093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032599
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498678
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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