A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416912



Internal ID21074465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78081901..78082900hg38UCSC Ensembl
chr8:78994136..78995135hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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