A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588590



Internal ID20961661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7849669..7850430hg38UCSC Ensembl
chr10:7891632..7892393hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237060
Samples
Known GenesTAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588590
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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