A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732138



Internal ID20508061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28267864..28268606hg38UCSC Ensembl
chr17:26594890..26595632hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732138
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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