A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1159013



Internal ID11975451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1368929..1368929hg38UCSC Ensembl
chr10:1411124..1411124hg19UCSC Ensembl
chr10:1401124..1401124hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38116
hg19116
hg18116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4212844
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1159013
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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