A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257691



Internal ID21400191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60604530..60613248hg38UCSC Ensembl
chr14:61071248..61079966hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg388719
hg198719
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730154
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257691
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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