A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073272



Internal ID20640312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44039256..44043898hg38UCSC Ensembl
chr21:45459137..45463779hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg384643
hg194643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543830
Supporting Variants
Samples
Known GenesTRAPPC10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073272
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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