A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573982



Internal ID20947053
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 StatusM
Merged Variants
Supporting Variantsnssv18266340
Samples
Known GenesGABRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573982
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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