A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277037



Internal ID20844077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11716366..11719485hg38UCSC Ensembl
chr8:11573875..11576994hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383120
hg193120
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572602
Supporting Variants
Samples
Known GenesGATA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277037
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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