A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325962



Internal ID20859096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157489441..157490950hg38UCSC Ensembl
chr1:157459231..157460740hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381510
hg191510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052698
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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