A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413804



Internal ID21071357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:463961..866903hg38UCSC Ensembl
chr6:463961..866903hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38402943
hg19402943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6041n223
Supporting Variantsnssv18226239
Samples
Known GenesEXOC2, HUS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413804
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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