A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514927



Internal ID20888282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95048601..95050600hg38UCSC Ensembl
chr15:95591830..95593829hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514927
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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