A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496825



Internal ID20870028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68312753..68320125hg38UCSC Ensembl
chr15:68605091..68612463hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg387373
hg197373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026259
Samples
Known GenesITGA11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496825
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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