A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319135



Internal ID20852227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84618901..84623600hg38UCSC Ensembl
chr1:85084584..85089283hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319135
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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