A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978892



Internal ID12979298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20016714..20030916hg38UCSC Ensembl
Innerchr10:20305643..20319845hg19UCSC Ensembl
Innerchr10:20345649..20359851hg18UCSC Ensembl
Innerchr10:20345649..20359851hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3814203
hg1914203
hg1814203
hg1714203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34798
Supporting Variants
SamplesNA12760
Known GenesPLXDC2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978892
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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