A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459237



Internal ID237254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19196832..19197592hg38UCSC Ensembl
chr7:19236455..19237215hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16993541
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459237
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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