A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3620202



Internal ID11794980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131939107..131939107hg38UCSC Ensembl
chr10:133752611..133752611hg19UCSC Ensembl
chr10:133602601..133602601hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3874
hg1974
hg1874
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1295798
Supporting Variants
SamplesHuRef
Known GenesPPP2R2D
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3620202
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