A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539604



Internal ID20912900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38193998..38206776hg38UCSC Ensembl
chr21:39566092..39578870hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3812779
hg1912779
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203949
Samples
Known GenesDSCR10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539604
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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