A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256357



Internal ID21398594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108311832..108413037hg38UCSC Ensembl
chr1:108854454..108955659hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38101206
hg19101206
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730086
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256357
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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