A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320186



Internal ID20853284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1584385..1637811hg38UCSC Ensembl
chr2:1588157..1641583hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3853427
hg1953427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205588
Samples
Known GenesPXDN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320186
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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