A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891858



Internal ID22666901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64929279..64937884hg38UCSC Ensembl
chr4:65794997..65803602hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg388606
hg198606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412772
Samples
Known GenesLOC401134
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891858
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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