A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993621



Internal ID20560661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74812000..74812640hg38UCSC Ensembl
chr11:74523045..74523685hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459125
Supporting Variants
Samples
Known GenesRNF169
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993621
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00084


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