A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457894



Internal ID235929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139103327..139103378hg38UCSC Ensembl
chr4:140024481..140024532hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16957522
Samples
Known GenesELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457894
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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