A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600800



Internal ID20973871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107138510..107138931hg38UCSC Ensembl
chr6:107459714..107460135hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600800
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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