A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017404



Internal ID21926747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144464052..144464111hg38UCSC Ensembl
chr7:144161145..144161204hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559296
Samples
Known GenesTPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017404
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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