A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905986



Internal ID22681180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:213167..386667hg38UCSC Ensembl
chr4:206956..380456hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38173501
hg19173501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418209
Samples
Known GenesZNF141, ZNF732, ZNF876P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905986
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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