A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635623



Internal ID6675735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104564498..104735876hg38UCSC Ensembl
chr14:105030835..105202213hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38171379
hg19171379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15114737
SamplesNA06984
Known GenesADSSL1, C14orf180, INF2, MIR4710, TMEM179
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635623
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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