A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588952



Internal ID20962023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58285924..58287086hg38UCSC Ensembl
chr10:60045684..60046846hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381163
hg191163
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222523
Samples
Known GenesCISD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588952
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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