A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410010



Internal ID21067563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85147885..85151660hg38UCSC Ensembl
chr6:85857603..85861378hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg383776
hg193776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410010
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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