A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316228



Internal ID20849306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21358468..21377564hg38UCSC Ensembl
chr1:21684961..21704057hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3819097
hg1919097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316228
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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