A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572478



Internal ID20945549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142120634..142123163hg38UCSC Ensembl
chr5:141500199..141502728hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg382530
hg192530
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267549
Samples
Known GenesNDFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572478
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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