A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15109391



Internal ID6319576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102248491..102294572hg38UCSC Ensembl
Innerchr14:102248991..102294072hg38UCSC Ensembl
Outerchr14:102247491..102295572hg38UCSC Ensembl
chr14:102714828..102760909hg19UCSC Ensembl
Innerchr14:102715328..102760409hg19UCSC Ensembl
Outerchr14:102713828..102761909hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3846082
hg1946082
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635549
Supporting Variants
SamplesNA19917
Known GenesMOK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15109391
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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