A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337445



Internal ID20994998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:155303311..155324993hg38UCSC Ensembl
chr2:156159823..156181505hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3821683
hg1921683
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337445
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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