A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068727



Internal ID20635767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15733570..15744168hg38UCSC Ensembl
chr21:17105889..17116487hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3810599
hg1910599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543679
Supporting Variants
Samples
Known GenesUSP25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068727
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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