A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794769



Internal ID21240107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88310166..88310166hg38UCSC Ensembl
chr14:88776510..88776510hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13692726
Samples
Known GenesKCNK10
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794769
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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