A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351676



Internal ID21009229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13520203..13613518hg38UCSC Ensembl
chr2:13660328..13753643hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3893316
hg1993316
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204875
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351676
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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