A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894863



Internal ID22669939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174586353..174586427hg38UCSC Ensembl
chr4:175507504..175507578hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894863
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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