A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576861



Internal ID20949932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32829529..32830949hg38UCSC Ensembl
chr17:31156547..31157967hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381421
hg191421
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244455
Samples
Known GenesMYO1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576861
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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