A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017015



Internal ID21926358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76885801..76886118hg38UCSC Ensembl
chr5:76181626..76181943hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549748
Samples
Known GenesS100Z
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017015
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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