A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865330



Internal ID22640265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13817486..13820085hg38UCSC Ensembl
chr12:13970420..13973019hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452077
Samples
Known GenesGRIN2B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865330
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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