A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455275



Internal ID233359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77879785..77890388hg38UCSC Ensembl
chr5:77175609..77186212hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3810604
hg1910604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968502
Samples
Known GenesLOC101929154
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455275
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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