A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502190



Internal ID20875433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81111167..81114083hg38UCSC Ensembl
chr15:81403508..81406424hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382917
hg192917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502190
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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