A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739669



Internal ID20515644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29388166..29388246hg38UCSC Ensembl
chr17:27715184..27715264hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739669
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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