A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926911



Internal ID22702139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138718230..138718473hg38UCSC Ensembl
chr7:138402975..138403218hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434697
Samples
Known GenesATP6V0A4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926911
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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