A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525434



Internal ID21849792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186490424..186491489hg38UCSC Ensembl
chr2:187355151..187356216hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg381066
hg191066
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110859
Supporting Variants
Samples
Known GenesZC3H15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525434
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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