A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569048



Internal ID20942119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93157592..93159486hg38UCSC Ensembl
chr5:92493298..92495192hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381895
hg191895
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5815n223
Supporting Variantsnssv18267696
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569048
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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