A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110059



Internal ID21512675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215962719..215963440hg38UCSC Ensembl
chr2:216827442..216828163hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667374
Supporting Variants
Samples
Known GenesMREG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110059
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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