A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337289



Internal ID20994842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143919601..143944700hg38UCSC Ensembl
chr2:144677168..144702267hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3825100
hg1925100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4146n223
Supporting Variantsnssv18207295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337289
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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