A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589290



Internal ID20962361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51550538..51716095hg38UCSC Ensembl
chr13:52124674..52290231hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38165558
hg19165558
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231915
Samples
Known GenesMIR4703, WDFY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589290
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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