A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011296



Internal ID21920639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168746259..168747034hg38UCSC Ensembl
chr5:168173264..168174039hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38776
hg19776
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575731
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011296
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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