A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428225



Internal ID21085778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50347952..50360865hg38UCSC Ensembl
chr8:51260512..51273425hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3812914
hg1912914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167529
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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