A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461122



Internal ID239083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112675157..112681653hg38UCSC Ensembl
chr5:112010854..112017350hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg386497
hg196497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16971960
Samples
Known GenesLOC102467216
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461122
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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