A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336546



Internal ID20994099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63770403..63790891hg38UCSC Ensembl
chr2:63997537..64018025hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3820489
hg1920489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336546
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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