A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15055841



Internal ID4748845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73226003..73226921hg38UCSC Ensembl
Innerchr14:73226053..73226871hg38UCSC Ensembl
Outerchr14:73225953..73226971hg38UCSC Ensembl
chr14:73692711..73693629hg19UCSC Ensembl
Innerchr14:73692761..73693579hg19UCSC Ensembl
Outerchr14:73692661..73693679hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634901
Supporting Variants
SamplesNA07347
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15055841
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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