A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636645



Internal ID21828692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8310732..8314671hg38UCSC Ensembl
chr19:8375616..8379555hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383940
hg193940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053798
Supporting Variants
Samples
Known GenesNDUFA7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636645
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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