A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935272



Internal ID22710611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96468473..96469990hg38UCSC Ensembl
chr14:96934810..96936327hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381518
hg191518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376176
Samples
Known GenesAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935272
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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