A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280956



Internal ID20490174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38771816..38790753hg38UCSC Ensembl
chr19:39262456..39281393hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3818938
hg1918938
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756804
Supporting Variants
Samples
Known GenesLGALS7, LGALS7B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280956
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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