A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595018



Internal ID20968089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64687816..64689038hg38UCSC Ensembl
chr17:62683934..62685156hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg381223
hg191223
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595018
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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