A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257127



Internal ID21397907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30210167..30214366hg38UCSC Ensembl
chr20:29444843..29449042hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730114
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257127
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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