A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593886



Internal ID20966957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15811975..15816252hg38UCSC Ensembl
chr10:15853974..15858251hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384278
hg194278
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv618n223
Supporting Variantsnssv18227314
Samples
Known GenesFAM188A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593886
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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