A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989149



Internal ID12981280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:28641109..28721209hg38UCSC Ensembl
Innerchr4:28642731..28722831hg19UCSC Ensembl
Innerchr4:28251829..28331929hg18UCSC Ensembl
Innerchr4:28319000..28399100hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3880101
hg1980101
hg1880101
hg1780101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34271
Supporting Variants
SamplesNA18956
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989149
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