A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008974



Internal ID21918317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1297961..1298046hg38UCSC Ensembl
chr8:1246217..1246302hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562377
Samples
Known GenesLOC286083
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008974
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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