A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257203



Internal ID21399016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197787654..197788854hg38UCSC Ensembl
chr1:197756784..197757984hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730195
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257203
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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