A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257979



Internal ID21399689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38773627..38789186hg38UCSC Ensembl
chr19:39264267..39279826hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3815560
hg1915560
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730253
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257979
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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