A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861079



Internal ID22636014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121866448..121868047hg38UCSC Ensembl
chr12:122304354..122305953hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465660
Samples
Known GenesHPD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861079
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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