A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001672



Internal ID21911015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59729639..59773254hg38UCSC Ensembl
chr8:60642198..60685813hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3843616
hg1943616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001672
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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