A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15089775



Internal ID1104977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85734690..85738553hg38UCSC Ensembl
Innerchr14:85734691..85738553hg38UCSC Ensembl
Outerchr14:85734690..85738554hg38UCSC Ensembl
chr14:86201034..86204897hg19UCSC Ensembl
Innerchr14:86201035..86204897hg19UCSC Ensembl
Outerchr14:86201034..86204898hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg383864
hg193864
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635202
Supporting Variants
SamplesHG00734
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15089775
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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