A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018495



Internal ID21927838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42018248..42018375hg38UCSC Ensembl
chr6:41985986..41986113hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562765
Samples
Known GenesCCND3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018495
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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