A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584942



Internal ID20958013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58500401..58500556hg38UCSC Ensembl
chr17:56577762..56577917hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245997
Samples
Known GenesMTMR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584942
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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