A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852231



Internal ID22627166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28268140..28270166hg38UCSC Ensembl
chr12:28421073..28423099hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg382027
hg192027
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460543
Samples
Known GenesCCDC91
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852231
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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