A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595907



Internal ID20968978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33413044..33413917hg38UCSC Ensembl
chr20:32000850..32001723hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251769
Samples
Known GenesSNTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595907
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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