A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034208



Internal ID21943551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18000265..18000367hg38UCSC Ensembl
chr17:17903579..17903681hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623720
Samples
Known GenesLRRC48
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034208
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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