A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588113



Internal ID20961184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100711818..100712512hg38UCSC Ensembl
chr13:101364072..101364766hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228016
Samples
Known GenesNALCN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588113
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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