A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596333



Internal ID20969404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52109356..52109587hg38UCSC Ensembl
chr20:50725895..50726126hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253277
Samples
Known GenesZFP64
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596333
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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