A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367017



Internal ID22592686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9615653..9617530hg38UCSC Ensembl
chr11:9637200..9639077hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381878
hg191878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924230
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367017
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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