A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15103760



Internal ID4287716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97627331..97638912hg38UCSC Ensembl
Innerchr14:97627331..97638912hg38UCSC Ensembl
Outerchr14:97626831..97639412hg38UCSC Ensembl
chr14:98093668..98105249hg19UCSC Ensembl
Innerchr14:98093668..98105249hg19UCSC Ensembl
Outerchr14:98093168..98105749hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3811582
hg1911582
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635448
Supporting Variants
SamplesHG03850
Known GenesLOC100129345
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15103760
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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