A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596600



Internal ID20969671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49259081..49259455hg38UCSC Ensembl
chr20:47875618..47875992hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252858
Samples
Known GenesZNFX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596600
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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