A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852949



Internal ID22627884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105313088..105327524hg38UCSC Ensembl
chr12:105706866..105721302hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3814437
hg1914437
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852949
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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