A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461435



Internal ID239387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138556116..138556451hg38UCSC Ensembl
chr5:137891805..137892140hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974074
Samples
Known GenesHSPA9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461435
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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