A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104368



Internal ID22013602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95752382..96071259hg38UCSC Ensembl
chr2:96418130..96737007hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38318878
hg19318878
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520303
Samples
Known GenesFAHD2CP, GPAT2, LINC00342
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104368
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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