A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002667



Internal ID21912010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142300171..142300282hg38UCSC Ensembl
chr5:141679736..141679847hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548185
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002667
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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