A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320986



Internal ID20854087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168253016..168265330hg38UCSC Ensembl
chr1:168222254..168234568hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3812315
hg1912315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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