A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322991



Internal ID20856106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:105425177..105462219hg38UCSC Ensembl
chr1:105967799..106004841hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3837043
hg1937043
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322991
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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