A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587570



Internal ID20960641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41744987..41749935hg38UCSC Ensembl
chr13:42319123..42324071hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg384949
hg194949
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223344
Samples
Known GenesVWA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587570
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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