A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001361



Internal ID21910704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43041096..43041230hg38UCSC Ensembl
chr8:42896239..42896373hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595191
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001361
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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