A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586969



Internal ID20960040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64111320..64112155hg38UCSC Ensembl
chr17:62188680..62189515hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38836
hg19836
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242636
Samples
Known GenesERN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586969
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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