A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425427



Internal ID21082980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8901010..8971378hg38UCSC Ensembl
chr8:8758520..8828888hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3870369
hg1970369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425427
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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