A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636957



Internal ID21829004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28725119..28725233hg38UCSC Ensembl
chr17:27052137..27052251hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022457
Supporting Variants
Samples
Known GenesTLCD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636957
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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