A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203964



Internal ID20771004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39829544..39885406hg38UCSC Ensembl
chr21:41201471..41257331hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3855863
hg1955861
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550301
Supporting Variants
Samples
Known GenesPCP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203964
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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