A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635266



Internal ID6675379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87833153..87954098hg38UCSC Ensembl
chr14:88299497..88420442hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38120946
hg19120946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15092134, essv15092135, essv15092137, essv15092136
SamplesHG00342, NA11840, NA12716, NA21141
Known GenesGALC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635266
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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