A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633880



Internal ID7020686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27541361..27618155hg38UCSC Ensembl
Innerchr14:27541379..27618137hg38UCSC Ensembl
Outerchr14:27541343..27618173hg38UCSC Ensembl
chr14:28010567..28087361hg19UCSC Ensembl
Innerchr14:28010585..28087343hg19UCSC Ensembl
Outerchr14:28010549..28087379hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3876795
hg1976795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv389e214
Supporting Variantsessv14947445, essv14947446, essv14947447
SamplesHG02628, HG04019, HG04200
Known GenesLINC00645
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633880
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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