A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988298



Internal ID7075569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143700691..143700892hg38UCSC Ensembl
chr5:143080256..143080457hg19UCSC Ensembl
chr5:143060449..143060650hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38202
hg19202
hg18202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3570330
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv988298
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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