A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335555



Internal ID20868748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90892968..90893334hg38UCSC Ensembl
chr1:91358525..91358891hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335555
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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