A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594862



Internal ID20967933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55874721..55875605hg38UCSC Ensembl
chr15:56166919..56167803hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241093
Samples
Known GenesNEDD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594862
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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