A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634913



Internal ID7021713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73561433..73573896hg38UCSC Ensembl
chr14:74028137..74040600hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3812464
hg1912464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15059508, essv15059505, essv15059514, essv15059510, essv15059509, essv15059513, essv15059502, essv15059503, essv15059506, essv15059511, essv15059512, essv15059507, essv15059504
SamplesNA10851, HG03821, NA12843, HG01188, NA21108, HG03793, HG00739, NA20895, HG00740, NA21124, HG00157, HG03743, NA12830
Known GenesACOT2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634913
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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