A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107503



Internal ID20674544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102840897..102842990hg38UCSC Ensembl
chr4:103762054..103764147hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382094
hg192094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379663
Supporting Variants
Samples
Known GenesUBE2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107503
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00044


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