A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988066



Internal ID12979311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19995420..20048189hg38UCSC Ensembl
Innerchr10:20284349..20337118hg19UCSC Ensembl
Innerchr10:20324355..20377124hg18UCSC Ensembl
Innerchr10:20324355..20377124hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3852770
hg1952770
hg1852770
hg1752770
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988066
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