A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426429



Internal ID21083982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47301538..47304547hg38UCSC Ensembl
chr8_gl000196_random:2375..5384hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383010
hg193010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426429
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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