A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429849



Internal ID21087402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66350101..66355046hg38UCSC Ensembl
chr8:67262336..67267281hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg384946
hg194946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169404
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429849
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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