A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004074



Internal ID21913417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132963829..132963884hg38UCSC Ensembl
chr5:132299521..132299576hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004074
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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