A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851573



Internal ID22626508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65178674..65185367hg38UCSC Ensembl
chr11:64946145..64952838hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg386694
hg196694
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466035
Samples
Known GenesCAPN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851573
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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