A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971190



Internal ID22746125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31632871..31651207hg38UCSC Ensembl
chr2:31857940..31876276hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg3818337
hg1918337
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404620
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971190
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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