A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069744



Internal ID20636784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30681778..30687740hg38UCSC Ensembl
chr21:32054096..32060058hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg385963
hg195963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069744
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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