A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005445



Internal ID21914788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:57149844..57198453hg38UCSC Ensembl
chr8:58062403..58111012hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3848610
hg1948610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005445
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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