A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1068695



Internal ID12231820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24882834..24882834hg38UCSC Ensembl
chr15:25127981..25127981hg19UCSC Ensembl
chr15:22679074..22679074hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3863
hg1963
hg1863
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4034799
SamplesHuRef
Known GenesSNRPN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1068695
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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