A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107501



Internal ID20674542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102834357..102834809hg38UCSC Ensembl
chr4:103755514..103755966hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391233
Supporting Variants
Samples
Known GenesUBE2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00012


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