A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320051



Internal ID20853149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229147423..229151313hg38UCSC Ensembl
chr1:229283170..229287060hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg383891
hg193891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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