A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319992



Internal ID20853090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:239311329..239312956hg38UCSC Ensembl
chr1:239474629..239476256hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg381628
hg191628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059432
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319992
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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