A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597532



Internal ID20970603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50175298..50175431hg38UCSC Ensembl
chr20:48791835..48791968hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597532
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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