A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740287



Internal ID20516262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149878838..149879001hg38UCSC Ensembl
chr7:149575927..149576090hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273557
Samples
Known GenesATP6V0E2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740287
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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