A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256191



Internal ID21400418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40024035..40038148hg38UCSC Ensembl
chr21:41395962..41410075hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3814114
hg1914114
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730189
Supporting Variants
SamplesNA19239
Known GenesDSCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256191
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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