A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257559



Internal ID21400157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149825866..149864067hg38UCSC Ensembl
chr1:149797419..149835633hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3838202
hg1938215
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730064
Supporting Variants
SamplesNA19239
Known GenesHIST2H2AA3, HIST2H2AA4, HIST2H2BC, HIST2H3A, HIST2H3C, HIST2H4A, HIST2H4B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257559
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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