A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560094



Internal ID20933165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134469918..134470566hg38UCSC Ensembl
chr5:133805609..133806257hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5940n223
Supporting Variantsnssv18267315
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560094
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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