A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597484



Internal ID20970555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36759684..36760192hg38UCSC Ensembl
chr20:35388087..35388595hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252563
Samples
Known GenesDSN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597484
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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