A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405358



Internal ID21062911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85608201..85612400hg38UCSC Ensembl
chr6:86317919..86322118hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6300n223
Supporting Variantsnssv18146058
Samples
Known GenesSYNCRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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