A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578533



Internal ID20951604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55621680..55628368hg38UCSC Ensembl
chr17:53699041..53705729hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg386689
hg196689
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578533
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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