A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067167



Internal ID20634207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25407834..25621719hg38UCSC Ensembl
chr20:25388470..25602355hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38213886
hg19213886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528988
Supporting Variants
Samples
Known GenesGINS1, NANP, NINL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067167
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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