A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068629



Internal ID20635669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14490455..14491120hg38UCSC Ensembl
chr21:15862776..15863441hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551340
Supporting Variants
Samples
Known GenesSAMSN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068629
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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