A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555753



Internal ID328903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62608725..62648352hg38UCSC Ensembl
chr2:62835860..62875487hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3839628
hg1939628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16914285
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555753
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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