A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634069



Internal ID21826116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29558296..29558418hg38UCSC Ensembl
chr17:27885314..27885436hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038587
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634069
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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