A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278219



Internal ID20845259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53747591..53747947hg38UCSC Ensembl
chr8:54660151..54660507hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562326
Supporting Variants
Samples
Known GenesATP6V1H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278219
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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