A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327149



Internal ID20860286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2750501..2761600hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3811100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv35n223
Supporting Variantsnssv18203511
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327149
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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