A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365471



Internal ID22591140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102449463..102546319hg38UCSC Ensembl
chr11:102320194..102417050hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3896857
hg1996857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920481
Supporting Variants
Samples
Known GenesMMP7, TMEM123
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365471
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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