A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1063968



Internal ID11880407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48709126..48709449hg38UCSC Ensembl
chr10:49917171..49917494hg19UCSC Ensembl
chr10:49587177..49587500hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38324
hg19324
hg18324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4091057
SamplesHuRef
Known GenesWDFY4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1063968
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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