A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402622



Internal ID21060175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27639790..27647580hg38UCSC Ensembl
chr6:27607569..27615359hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg387791
hg197791
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236732
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402622
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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