A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409028



Internal ID21066581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70152015..70210200hg38UCSC Ensembl
chr6:70861907..70919903hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3858186
hg1957997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227846
Samples
Known GenesCOL19A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409028
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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