A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855726



Internal ID22630661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102837296..102838695hg38UCSC Ensembl
chr11:102708027..102709426hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457059
Samples
Known GenesMMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855726
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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