A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152437



Internal ID20719477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14279786..14296665hg38UCSC Ensembl
chr7:14319411..14336290hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3816880
hg1916880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618477
Supporting Variants
Samples
Known GenesDGKB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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