A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258595



Internal ID21399741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149820939..149862254hg38UCSC Ensembl
chr1:149792494..149833820hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3841316
hg1941327
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730064
Supporting Variants
SamplesHG00733
Known GenesHIST2H2AA3, HIST2H2AA4, HIST2H2BC, HIST2H3A, HIST2H3C, HIST2H4A, HIST2H4B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258595
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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