A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633940



Internal ID7020744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29973537..30006827hg38UCSC Ensembl
Innerchr14:29973560..30006805hg38UCSC Ensembl
Outerchr14:29973515..30006850hg38UCSC Ensembl
chr14:30442743..30476033hg19UCSC Ensembl
Innerchr14:30442766..30476011hg19UCSC Ensembl
Outerchr14:30442721..30476056hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3833291
hg1933291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14951912
SamplesHG02235
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633940
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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