A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256769



Internal ID21399921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60604530..60613253hg38UCSC Ensembl
chr14:61071248..61079971hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg388724
hg198724
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730154
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256769
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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