A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327059



Internal ID20860196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38474001..38478900hg38UCSC Ensembl
chr1:38939673..38944572hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327059
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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