A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377891



Internal ID21035444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55400101..55402900hg38UCSC Ensembl
chr4:56266268..56269067hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5271n223
Supporting Variantsnssv18118359
Samples
Known GenesTMEM165
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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