A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16924602



Internal ID17153
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 StatusS
Merged Variantsnsv5560929
Supporting Variants
Samples
Known GenesMREG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16924602
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.013737


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