A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238393



Internal ID20805433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96455970..96457073hg38UCSC Ensembl
chr14:96922307..96923410hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581081
Supporting Variants
Samples
Known GenesAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238393
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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