A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361791



Internal ID22587460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102837260..102838699hg38UCSC Ensembl
chr11:102707991..102709430hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381440
hg191440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919677
Supporting Variants
Samples
Known GenesMMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361791
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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