A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995855



Internal ID20562895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97923006..98008548hg38UCSC Ensembl
chr11:97794006..97879276hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3885543
hg1985271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463868
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995855
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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