A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500955



Internal ID277872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42629398..42654357hg38UCSC Ensembl
chr13:43203534..43228493hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3824960
hg1924960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17687230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500955
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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