A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102503



Internal ID22011738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158332476..158362096hg38UCSC Ensembl
chr2:159188988..159218608hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3829621
hg1929621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522944
Samples
Known GenesCCDC148
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102503
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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