A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761672



Internal ID20537532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97194143..97546003hg38UCSC Ensembl
chr2:97859880..98162466hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38351861
hg19302587
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281320
Samples
Known GenesANKRD36, ANKRD36B, LOC100506076, LOC100506123
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761672
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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