A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372673



Internal ID21030226
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 StatusM
Merged Variants
Supporting Variantsnssv18100630
Samples
Known GenesCDCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372673
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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