A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318037



Internal ID20851128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223035215..223037620hg38UCSC Ensembl
chr1:223208557..223210962hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg382406
hg192406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318037
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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