A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18118544



Internal ID20685584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62428675..62429107hg38UCSC Ensembl
chr4:63294393..63294825hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6388956
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18118544
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00071


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