A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110967



Internal ID20678007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154607230..154607772hg38UCSC Ensembl
chr4:155528382..155528924hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391477
Supporting Variants
Samples
Known GenesFGG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110967
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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