A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990704



Internal ID20557744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38743890..38744319hg38UCSC Ensembl
chr11:38765440..38765869hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463632
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990704
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0008


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