A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350932



Internal ID22576601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102432853..102436753hg38UCSC Ensembl
chr11:102303584..102307484hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg383901
hg193901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922583
Supporting Variants
Samples
Known GenesTMEM123
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350932
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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