A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888222



Internal ID22663224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55400568..55402824hg38UCSC Ensembl
chr4:56266735..56268991hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382257
hg192257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413228
Samples
Known GenesTMEM165
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888222
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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