A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588161



Internal ID20961232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21139648..21140031hg38UCSC Ensembl
chr17:21042961..21043344hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241537
Samples
Known GenesDHRS7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588161
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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