A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18120566



Internal ID20687606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:944505..949434hg38UCSC Ensembl
chr4:938293..943222hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg384930
hg194930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361382
Supporting Variants
Samples
Known GenesTMEM175
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18120566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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