A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634873



Internal ID7021673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71141784..71146517hg38UCSC Ensembl
Innerchr14:71141784..71146517hg38UCSC Ensembl
Outerchr14:71141648..71146672hg38UCSC Ensembl
chr14:71608501..71613234hg19UCSC Ensembl
Innerchr14:71608501..71613234hg19UCSC Ensembl
Outerchr14:71608365..71613389hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg384734
hg194734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15053931
SamplesHG01440
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634873
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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