A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936350



Internal ID22711703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9578298..9586330hg38UCSC Ensembl
chr17:9481615..9489647hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg388033
hg198033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377844
Samples
Known GenesWDR16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936350
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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