A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591594



Internal ID20964665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64552900..64553378hg38UCSC Ensembl
chr17:62549018..62549496hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243279
Samples
Known GenesSMURF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591594
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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