A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587854



Internal ID20960925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40997440..40997869hg38UCSC Ensembl
chr13:41571576..41572005hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236299
Samples
Known GenesELF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587854
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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