A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565373



Internal ID6690069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:9362998..9365943hg38UCSC Ensembl
Outerchr10:9404961..9407906hg19UCSC Ensembl
Outerchr10:9444967..9447912hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382400
hg192400
hg182400
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1002404
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565373
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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