A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496426



Internal ID20869628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83539061..83539941hg38UCSC Ensembl
chr15:84207813..84208693hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027190
Samples
Known GenesSH3GL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496426
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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