A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908961



Internal ID22684171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5482638..5482692hg38UCSC Ensembl
chr12:5591804..5591858hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363517
Samples
Known GenesNTF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908961
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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