A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572519



Internal ID20945590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82189623..82190552hg38UCSC Ensembl
chr5:81485442..81486371hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38930
hg19930
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5796n223
Supporting Variantsnssv18269622
Samples
Known GenesATG10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572519
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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