A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368923



Internal ID22594592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102719416..102719416hg38UCSC Ensembl
chr11:102590147..102590147hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979883
Supporting Variants
Samples
Known GenesMMP8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368923
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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