A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584656



Internal ID20957727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41974135..41975226hg38UCSC Ensembl
chr13:42548271..42549362hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg381092
hg191092
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1812n223
Supporting Variantsnssv18221188
Samples
Known GenesVWA8-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584656
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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