A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634129



Internal ID7020933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38740172..38744614hg38UCSC Ensembl
Innerchr14:38740172..38744614hg38UCSC Ensembl
Outerchr14:38739939..38744869hg38UCSC Ensembl
chr14:39209376..39213818hg19UCSC Ensembl
Innerchr14:39209376..39213818hg19UCSC Ensembl
Outerchr14:39209143..39214073hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg384443
hg194443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14973868
SamplesHG00708
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634129
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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