A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591628



Internal ID20964699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37295642..37296606hg38UCSC Ensembl
chr17:35652565..35653528hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38965
hg19964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242225
Samples
Known GenesACACA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591628
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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