A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595837



Internal ID20968908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40891378..40892330hg38UCSC Ensembl
chr22:41287382..41288334hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38953
hg19953
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4706n223
Supporting Variantsnssv18255604
Samples
Known GenesXPNPEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595837
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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