A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850672



Internal ID22625607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102449445..102521529hg38UCSC Ensembl
chr11:102320176..102392260hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3872085
hg1972085
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459011
Samples
Known GenesMMP7, TMEM123
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850672
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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