A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258332



Internal ID21398870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149843172..149855461hg38UCSC Ensembl
chr1:149814739..149827027hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3812290
hg1912289
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730064
Supporting Variants
SamplesHG00731
Known GenesHIST2H2AA3, HIST2H2AA4, HIST2H2BC, HIST2H3A, HIST2H3C
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258332
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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