A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068636



Internal ID20635676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14558617..14562138hg38UCSC Ensembl
chr21:15930938..15934459hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg383522
hg193522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537484
Supporting Variants
Samples
Known GenesSAMSN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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