A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026111



Internal ID20593151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61613947..61628073hg38UCSC Ensembl
chr15:61906146..61920272hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3814127
hg1914127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512798
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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