A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590257



Internal ID20963328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59135102..59139131hg38UCSC Ensembl
chr17:57212463..57216492hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg384030
hg194030
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243721
Samples
Known GenesMIR454, SKA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590257
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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