A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968797



Internal ID22743732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106481874..106482237hg38UCSC Ensembl
chr1:107024496..107024859hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357513
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968797
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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