A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257463



Internal ID21398873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30392219..30410704hg38UCSC Ensembl
chr20:29626895..29645380hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3818486
hg1918486
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730114
Supporting Variants
SamplesHG00731
Known GenesFRG1B, MLLT10P1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257463
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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