A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512327



Internal ID20885660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66860781..66861647hg38UCSC Ensembl
chr15:67153119..67153985hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025436
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512327
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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