A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865560



Internal ID22640495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93510139..93511538hg38UCSC Ensembl
chr12:93903915..93905314hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865560
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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