A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563611



Internal ID21887966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43141672..43144352hg38UCSC Ensembl
chr7:43181271..43183951hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382681
hg192681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012799
Supporting Variants
Samples
Known GenesHECW1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563611
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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