A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561914



Internal ID20934985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4623508..4624581hg38UCSC Ensembl
chr4:4625235..4626308hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg381074
hg191074
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266321
Samples
Known GenesSTX18-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561914
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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