A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407336



Internal ID21064889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15022533..15029604hg38UCSC Ensembl
chr6:15022764..15029835hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg387072
hg197072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141014
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407336
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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