A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569922



Internal ID20942993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113772743..113772956hg38UCSC Ensembl
chr3:113491590..113491803hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259251
Samples
Known GenesATP6V1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569922
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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