A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026667



Internal ID20593707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74503068..74516468hg38UCSC Ensembl
chr15:74795409..74808809hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3813401
hg1913401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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