A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258459



Internal ID21399402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34547914..34555190hg38UCSC Ensembl
chr14:35017120..35024396hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg387277
hg197277
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730050
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258459
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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