A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571634



Internal ID21763677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125213113..125266516hg38UCSC Ensembl
chr6:125534259..125587662hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3853404
hg1953404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001160
Supporting Variants
Samples
Known GenesTPD52L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571634
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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