A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007111



Internal ID21916454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41683252..41684538hg38UCSC Ensembl
chr8:41540770..41542056hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381287
hg191287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584555
Samples
Known GenesANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007111
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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