A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020824



Internal ID21930167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39015459..39015540hg38UCSC Ensembl
chr17:37171712..37171793hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626998
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020824
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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