A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15106766



Internal ID1190212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98711855..98730148hg38UCSC Ensembl
chr14:99178192..99196485hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3818294
hg1918294
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635471
Supporting Variants
SamplesHG01066
Known GenesC14orf177
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15106766
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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