A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433876



Internal ID21091429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:129691232..129691844hg38UCSC Ensembl
chr8:130703478..130704090hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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