A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591992



Internal ID20965063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96915240..96916203hg38UCSC Ensembl
chr10:98674997..98675960hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38964
hg19964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229286
Samples
Known GenesLCOR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591992
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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