A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430586



Internal ID21088139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:57003801..57017900hg38UCSC Ensembl
chr8:57916360..57930459hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3814100
hg1914100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7357n223
Supporting Variantsnssv18169238
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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