A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256376



Internal ID21398601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:49623982..49646321hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3822340
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730092
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256376
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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