A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699454



Internal ID21221294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100378662..100378994hg38UCSC Ensembl
chr14:100844999..100845331hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794059
Supporting Variants
Samples
Known GenesWDR25
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699454
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.703125


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