A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928960



Internal ID22704206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23063638..23063707hg38UCSC Ensembl
chr14:23532847..23532916hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380347
Samples
Known GenesACIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928960
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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