A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979769



Internal ID12980723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153764521..153948014hg38UCSC Ensembl
Innerchr7:153461606..153645099hg19UCSC Ensembl
Innerchr7:153092539..153276032hg18UCSC Ensembl
Innerchr7:152899254..153082747hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38183494
hg19183494
hg18183494
hg17183494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34787
Supporting Variants
SamplesNA18623
Known GenesDPP6
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979769
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