A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295619



Internal ID20504837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63340343..63340537hg38UCSC Ensembl
chr20:61971695..61971889hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732825
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295619
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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