A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003668



Internal ID21913011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149121965..149123541hg38UCSC Ensembl
chr5:148501528..148503104hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381577
hg191577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561410
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003668
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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