A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980474



Internal ID12635796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2650601..3091456hg38UCSC Ensembl
Innerchr10:2692793..3133648hg19UCSC Ensembl
Innerchr10:2682793..3123648hg18UCSC Ensembl
Innerchr10:2682793..3123648hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38440856
hg19440856
hg18440856
hg17440856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34832
Supporting Variants
SamplesNA19201
Known GenesPFKP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980474
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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