A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322241



Internal ID20855352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19541921..19579082hg38UCSC Ensembl
chr1:19868415..19905576hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3837162
hg1937162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18055964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322241
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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