A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3583295



Internal ID6707991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75352103..75352103hg38UCSC Ensembl
chr10:77111861..77111861hg19UCSC Ensembl
chr10:76781867..76781867hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38229
hg19229
hg18229
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991439
Supporting Variants
SamplesHuRef
Known GenesZNF503-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3583295
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