A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492670



Internal ID269877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138743941..138744059hg38UCSC Ensembl
chr7:138428686..138428804hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17006294
Samples
Known GenesATP6V0A4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492670
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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