A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557422



Internal ID20930493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10505844..10507183hg38UCSC Ensembl
chr5:10505956..10507295hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381340
hg191340
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5638n223
Supporting Variantsnssv18266493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557422
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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