A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635412



Internal ID7022211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95994979..95999020hg38UCSC Ensembl
Innerchr14:95994979..95999020hg38UCSC Ensembl
Outerchr14:95994654..95999330hg38UCSC Ensembl
chr14:96461316..96465357hg19UCSC Ensembl
Innerchr14:96461316..96465357hg19UCSC Ensembl
Outerchr14:96460991..96465667hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384042
hg194042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103424
SamplesHG00556
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635412
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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