A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900916



Internal ID22676063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82798094..82799119hg38UCSC Ensembl
chr5:82093913..82094938hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg381026
hg191026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900916
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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