A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025809



Internal ID20592849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76772064..76772796hg38UCSC Ensembl
chr15:77064405..77065137hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500553
Supporting Variants
Samples
Known GenesSCAPER
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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