A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258739



Internal ID21399437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95431186..95460314hg38UCSC Ensembl
chr2:96096934..96126062hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg3829129
hg1929129
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730053
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258739
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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