A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399062



Internal ID21056615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49876549..49889789hg38UCSC Ensembl
chr6:49844262..49857502hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3813241
hg1913241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224578
Samples
Known GenesCRISP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399062
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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