A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541016



Internal ID20914301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39870722..39871092hg38UCSC Ensembl
chr21:41242648..41243018hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072664
Samples
Known GenesPCP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541016
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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