A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025091



Internal ID21934434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10879751..10880601hg38UCSC Ensembl
chr17:10783068..10783918hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38851
hg19851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025091
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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