A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206039



Internal ID20773079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:28991701..29012300hg38UCSC Ensembl
chr21:30364022..30384621hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3820600
hg1920600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553813
Supporting Variants
Samples
Known GenesLTN1, RWDD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206039
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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