A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568978



Internal ID20942049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57219262..57220497hg38UCSC Ensembl
chr5:56515089..56516324hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381236
hg191236
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268897
Samples
Known GenesGPBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568978
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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