A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328799



Internal ID20861949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229409856..229410890hg38UCSC Ensembl
chr1:229545603..229546637hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg381035
hg191035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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