A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432654



Internal ID21090207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137180356..137181051hg38UCSC Ensembl
chr8:138192599..138193294hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432654
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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