A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1589394



Internal ID12405829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1327430..1327520hg38UCSC Ensembl
chr10:1369625..1369715hg19UCSC Ensembl
chr10:1359625..1359715hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3891
hg1991
hg1891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4058557
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1589394
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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