A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938701



Internal ID22714085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28329940..28330115hg38UCSC Ensembl
chr17:26656966..26657141hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386920
Samples
Known GenesIFT20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938701
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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