A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498463



Internal ID20871673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94186016..94283892hg38UCSC Ensembl
chr15:94729245..94827121hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3897877
hg1997877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498463
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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