A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596661



Internal ID20969732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50938500..50938986hg38UCSC Ensembl
chr20:49555037..49555523hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4486n223
Supporting Variantsnssv18252619
Samples
Known GenesDPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596661
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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