A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637494



Internal ID21829541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47700165..47700320hg38UCSC Ensembl
chr17:45777531..45777686hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035108
Supporting Variants
Samples
Known GenesTBKBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637494
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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