A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976996



Internal ID22751931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91059396..91060231hg38UCSC Ensembl
chr10:92819153..92819988hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38836
hg19836
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353400
Samples
Known GenesLINC00502
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976996
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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