A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031447



Internal ID21940790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83205558..83205894hg38UCSC Ensembl
chr17:81153327..81153663hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031447
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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