A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15023214



Internal ID4297664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57025298..57040152hg38UCSC Ensembl
Innerchr14:57025298..57040152hg38UCSC Ensembl
Outerchr14:57024798..57040652hg38UCSC Ensembl
chr14:57492016..57506870hg19UCSC Ensembl
Innerchr14:57492016..57506870hg19UCSC Ensembl
Outerchr14:57491516..57507370hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3814855
hg1914855
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634601
Supporting Variants
SamplesHG03857
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15023214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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