A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329080



Internal ID20862231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244239041..244240344hg38UCSC Ensembl
chr1:244402343..244403646hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg381304
hg191304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329080
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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