A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589085



Internal ID20962156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12873953..12874168hg38UCSC Ensembl
chr10:12915953..12916168hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589085
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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