A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588195



Internal ID20961266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10443856..10458286hg38UCSC Ensembl
chr17:10347173..10361603hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3814431
hg1914431
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240958
Samples
Known GenesMYH4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588195
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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