A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266340



Internal ID20833380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47067544..47070629hg38UCSC Ensembl
chr4:47069561..47072646hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg383086
hg193086
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573982
Supporting Variants
Samples
Known GenesGABRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266340
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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