A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599283



Internal ID20972354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34589480..34590446hg38UCSC Ensembl
chr20:33177284..33178250hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38967
hg19967
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252452
Samples
Known GenesPIGU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599283
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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