A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458906



Internal ID236926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96911971..96922016hg38UCSC Ensembl
chr5:96247675..96257720hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3810046
hg1910046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16971039
Samples
Known GenesERAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458906
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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