A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1670054



Internal ID12486486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1675047..1675047hg38UCSC Ensembl
chr10:1717241..1717241hg19UCSC Ensembl
chr10:1707241..1707241hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3866
hg1966
hg1866
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4077679
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1670054
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer