A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1372493



Internal ID12188930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1464642..1464708hg38UCSC Ensembl
chr10:1506837..1506903hg19UCSC Ensembl
chr10:1496837..1496903hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3867
hg1967
hg1867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4342203
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1372493
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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