A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635613



Internal ID6675725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103925336..103928365hg38UCSC Ensembl
Innerchr14:103925836..103927865hg38UCSC Ensembl
Outerchr14:103924336..103929365hg38UCSC Ensembl
chr14:104391673..104394702hg19UCSC Ensembl
Innerchr14:104392173..104394202hg19UCSC Ensembl
Outerchr14:104390673..104395702hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg383030
hg193030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15114686
SamplesHG02944
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635613
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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