A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488889



Internal ID266183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24430289..24433251hg38UCSC Ensembl
chr7:24469908..24472870hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg382963
hg192963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488889
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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