A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350716



Internal ID22576385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44608367..44611181hg38UCSC Ensembl
chr11:44629917..44632731hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382815
hg192815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918291
Supporting Variants
Samples
Known GenesCD82
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350716
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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