A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032040



Internal ID21941383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28329941..28330118hg38UCSC Ensembl
chr17:26656967..26657144hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621817
Samples
Known GenesIFT20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032040
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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