A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010678



Internal ID6722768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47485818..47485869hg38UCSC Ensembl
chr4:47487835..47487886hg19UCSC Ensembl
chr4:47182592..47182643hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3572881
SamplesHuRef
Known GenesATP10D
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010678
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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