A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592373



Internal ID20965444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42812612..42813131hg38UCSC Ensembl
chr17:40964630..40965149hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243025
Samples
Known GenesBECN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592373
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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