A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402798



Internal ID21060351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37186373..37186713hg38UCSC Ensembl
chr6:37154149..37154489hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225312
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402798
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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