A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570387



Internal ID20943458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79310868..79311272hg38UCSC Ensembl
chr5:78606691..78607095hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270293
Samples
Known GenesJMY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570387
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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