A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563173



Internal ID20936244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65269791..65271336hg38UCSC Ensembl
chr5:64565618..64567163hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg381546
hg191546
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269181
Samples
Known GenesADAMTS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563173
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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