A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932889



Internal ID22708194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95882974..95883029hg38UCSC Ensembl
chr14:96349311..96349366hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386709
Samples
Known GenesLINC00617
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932889
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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