A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3573397



Internal ID7044779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23111808..23111861hg38UCSC Ensembl
chr10:23400737..23400790hg19UCSC Ensembl
chr10:23440743..23440796hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv987760
Supporting Variants
SamplesHuRef
Known GenesMSRB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3573397
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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