A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257101



Internal ID21398926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:138246675..138251784hg38UCSC Ensembl
chr2:139004245..139009354hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg385110
hg195110
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730094
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257101
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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