A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356127



Internal ID21013680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122363278..122363874hg38UCSC Ensembl
chr3:122082125..122082721hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095201
Samples
Known GenesCCDC58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356127
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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