A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570703



Internal ID20943774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:79131783..79132201hg38UCSC Ensembl
chr4:80052937..80053355hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265331
Samples
Known GenesLINC01088
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570703
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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