A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398458



Internal ID21056011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40366325..40366679hg38UCSC Ensembl
chr6:40334064..40334418hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142732
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398458
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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