A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005750



Internal ID21915093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176394484..176394625hg38UCSC Ensembl
chr5:175821485..175821626hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571266
Samples
Known GenesCLTB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005750
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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