A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858567



Internal ID22633502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71646581..71649303hg38UCSC Ensembl
chr12:72040361..72043083hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg382723
hg192723
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451295
Samples
Known GenesZFC3H1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858567
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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