A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594122



Internal ID20967193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114641076..114641370hg38UCSC Ensembl
chr10:116400835..116401129hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223005
Samples
Known GenesABLIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594122
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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