A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027002



Internal ID20594042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88568424..88568779hg38UCSC Ensembl
chr15:89111655..89112010hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027002
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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