A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003821



Internal ID21913164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47702049..47702101hg38UCSC Ensembl
chr8:48614611..48614663hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580163
Samples
Known GenesSPIDR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003821
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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