A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269022



Internal ID20478240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29833690..29833892hg38UCSC Ensembl
chr17:28160708..28160910hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741124
Supporting Variants
Samples
Known GenesSSH2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269022
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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