A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100630



Internal ID20667670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45087921..45088319hg38UCSC Ensembl
chr3:45129413..45129811hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372673
Supporting Variants
Samples
Known GenesCDCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100630
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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