A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3573831



Internal ID7045213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86524712..86524712hg38UCSC Ensembl
chr10:88284469..88284469hg19UCSC Ensembl
chr10:88274449..88274449hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3893
hg1993
hg1893
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001048
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3573831
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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