A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014271



Internal ID21923614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:104032112..104036904hg38UCSC Ensembl
chr5:103367813..103372605hg19UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg384793
hg194793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014271
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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