A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995804



Internal ID20562844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97538909..97690647hg38UCSC Ensembl
chr11:97409909..97561647hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38151739
hg19151739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466618
Supporting Variants
Samples
Known GenesMIR7976
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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