A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025516



Internal ID20592557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77962414..77967516hg38UCSC Ensembl
chr15:78254756..78259858hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg385103
hg195103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514325
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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