A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905998



Internal ID22681192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116918128..116954413hg38UCSC Ensembl
chr5:116253824..116290109hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3836286
hg1936286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419212
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905998
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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