A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502595



Internal ID20875841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81513008..81513457hg38UCSC Ensembl
chr16:81546613..81547062hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032889
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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