A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4149316



Internal ID11085168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1229703..1229703hg38UCSC Ensembl
chr10:1275643..1275643hg19UCSC Ensembl
chr10:1265643..1265643hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38150
hg19150
hg18150
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1227692
Supporting Variants
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4149316
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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