A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575887



Internal ID20948958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94585143..94585778hg38UCSC Ensembl
chr13:95237397..95238032hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38636
hg19636
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234936
Samples
Known GenesTGDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575887
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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