A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672001



Internal ID21620306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236356297..236359083hg38UCSC Ensembl
chr2:237264940..237267726hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg382787
hg192787
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110289
Samples
Known GenesIQCA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672001
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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