A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15107069



Internal ID5814072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99105811..99113530hg38UCSC Ensembl
Innerchr14:99105811..99113530hg38UCSC Ensembl
Outerchr14:99105311..99114030hg38UCSC Ensembl
chr14:99572148..99579867hg19UCSC Ensembl
Innerchr14:99572148..99579867hg19UCSC Ensembl
Outerchr14:99571648..99580367hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg387720
hg197720
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635479
Supporting Variants
SamplesNA19190
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15107069
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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