A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512995



Internal ID20886335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97144774..97148866hg38UCSC Ensembl
chr15:97688004..97692096hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg384093
hg194093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027945
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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