A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847769



Internal ID22622704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20099172..20105171hg38UCSC Ensembl
chr12:20252106..20258105hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462420, nssv17466959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847769
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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