A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939510



Internal ID22714904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95714413..95714526hg38UCSC Ensembl
chr12:96108191..96108304hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366268
Samples
Known GenesNTN4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939510
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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