A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593161



Internal ID20966232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13519955..13527355hg38UCSC Ensembl
chr10:13561955..13569355hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg387401
hg197401
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593161
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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