A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977961



Internal ID22752896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74745540..74746423hg38UCSC Ensembl
chr10:76505298..76506181hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38884
hg19884
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355625
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977961
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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