A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256594



Internal ID21399068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:146194656..149250192hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383055537
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730271
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256594
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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