A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024308



Internal ID21933651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81023872..81023931hg38UCSC Ensembl
chr17:78997672..78997731hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634834
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024308
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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