A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316464



Internal ID20849543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205641159..205643782hg38UCSC Ensembl
chr1:205610287..205612910hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382624
hg192624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316464
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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