A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238395



Internal ID20805435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96465860..96466236hg38UCSC Ensembl
chr14:96932197..96932573hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589283
Supporting Variants
Samples
Known GenesAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238395
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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