A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581771



Internal ID20954842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40143454..40145182hg38UCSC Ensembl
chr17:38299707..38301435hg19UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg381729
hg191729
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242944
Samples
Known GenesCASC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581771
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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