A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899015



Internal ID22674141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37341863..37342022hg38UCSC Ensembl
chr5:37341965..37342124hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415139
Samples
Known GenesNUP155
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899015
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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