A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007556



Internal ID21916899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148844686..148845104hg38UCSC Ensembl
chr5:148224249..148224667hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007556
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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