A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991694



Internal ID20558734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45242322..45242900hg38UCSC Ensembl
chr11:45263873..45264451hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462327
Supporting Variants
Samples
Known GenesSYT13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991694
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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