A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597435



Internal ID20970506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50669215..50768005hg38UCSC Ensembl
chr20:49285752..49384542hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3898791
hg1998791
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4484n223
Supporting Variantsnssv18252605
Samples
Known GenesPARD6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597435
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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