A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454202



Internal ID21111755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6237182..6258249hg38UCSC Ensembl
chr10:6279145..6300212hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3821068
hg1921068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982784
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454202
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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