A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492664



Internal ID269871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144445552..144447247hg38UCSC Ensembl
chr7:144142645..144144340hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg381696
hg191696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492664
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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