A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599125



Internal ID20972196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34444398..34444838hg38UCSC Ensembl
chr20:33032203..33032643hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252444
Samples
Known GenesITCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599125
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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