A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116028



Internal ID20683068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38713105..38721384hg38UCSC Ensembl
chr4:38714726..38723005hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg388280
hg198280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394988
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116028
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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