A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560542



Internal ID20933613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53513589..53514557hg38UCSC Ensembl
chr5:52809419..52810387hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5757n223
Supporting Variantsnssv18269051
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560542
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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