A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401036



Internal ID21058589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1922701..1927400hg38UCSC Ensembl
chr6:1922935..1927634hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230462
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401036
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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