A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602721



Internal ID6642977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153311288..153313890hg38UCSC Ensembl
Innerchr4:153311338..153313715hg38UCSC Ensembl
Outerchr4:153311204..153313974hg38UCSC Ensembl
chr4:154232440..154235042hg19UCSC Ensembl
Innerchr4:154232490..154234867hg19UCSC Ensembl
Outerchr4:154232356..154235126hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382603
hg192603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11655708, essv11655719, essv11655716, essv11655706, essv11655705, essv11655713, essv11655711, essv11655717, essv11655715, essv11655704, essv11655714, essv11655718, essv11655707, essv11655712, essv11655709, essv11655710
SamplesHG02890, HG03058, NA19209, NA20294, NA19923, HG02583, NA20340, HG02577, NA19129, HG03433, HG02052, NA19403, HG03556, NA20287, NA19099, NA20359
Known GenesTRIM2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602721
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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