A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498979



Internal ID20872194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26412055..26413920hg38UCSC Ensembl
chr15:26657202..26659067hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381866
hg191866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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