A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544880



Internal ID20918118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39903643..39905823hg38UCSC Ensembl
chr21:41275568..41277748hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg382181
hg192181
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203965
Samples
Known GenesPCP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544880
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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