A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862477



Internal ID22637412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31995679..32000047hg38UCSC Ensembl
chr12:32148613..32152981hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg384369
hg194369
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862477
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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