A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560929



Internal ID333922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215962713..215963441hg38UCSC Ensembl
chr2:216827436..216828164hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16924602
Samples
Known GenesMREG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560929
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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