A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329372



Internal ID20862524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234708381..234717684hg38UCSC Ensembl
chr1:234844128..234853431hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg389304
hg199304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058819
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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