A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556892



Internal ID20929963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14938036..14938721hg38UCSC Ensembl
chr5:14938145..14938830hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268669
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556892
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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