A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323438



Internal ID20856556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226922179..226923001hg38UCSC Ensembl
chr1:227109880..227110702hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38823
hg19823
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202713
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323438
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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