A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362652



Internal ID22588321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85344899..85349942hg38UCSC Ensembl
chr11:85055943..85060986hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg385044
hg195044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918176
Supporting Variants
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362652
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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