A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110531



Internal ID20677571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:128614588..128614954hg38UCSC Ensembl
chr4:129535743..129536109hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389006
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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