A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588364



Internal ID20961435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119854295..119854545hg38UCSC Ensembl
chr10:121613807..121614057hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234780
Samples
Known GenesMCMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588364
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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