A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415783



Internal ID21073336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35168466..35199092hg38UCSC Ensembl
chr8:35025984..35056610hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3830627
hg1930627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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