A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256129



Internal ID21399813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34540845..34562456hg38UCSC Ensembl
chr14:35010051..35031662hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3821612
hg1921612
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730050
Supporting Variants
SamplesNA19238
Known GenesSNX6
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256129
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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