A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028973



Internal ID20596013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31714675..31726499hg38UCSC Ensembl
chr16:31725996..31737820hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3811825
hg1911825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509289
Supporting Variants
Samples
Known GenesZNF720
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028973
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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