A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15137478



Internal ID5817844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106842095..106881350hg38UCSC Ensembl
chr14:107250311..107289542hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3839256
hg1939232
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635714
Supporting Variants
SamplesNA19197
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15137478
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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