A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000761



Internal ID6712903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29423217..29423791hg38UCSC Ensembl
chr10:29712146..29712720hg19UCSC Ensembl
chr10:29752152..29752726hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38575
hg19575
hg18575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3585437
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000761
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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