A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1595476



Internal ID12411911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1593035..1593161hg38UCSC Ensembl
chr10:1635230..1635356hg19UCSC Ensembl
chr10:1625230..1625356hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38127
hg19127
hg18127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4093615
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1595476
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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