A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4034799



Internal ID11727075
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1068695
Supporting Variants
SamplesHuRef
Known GenesSNRPN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4034799
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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