A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863819



Internal ID22638754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76924077..76944095hg38UCSC Ensembl
chr12:77317857..77337875hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3820019
hg1920019
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863819
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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