A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987067



Internal ID12978306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36267143..36303343hg38UCSC Ensembl
Innerchr14:36736349..36772549hg19UCSC Ensembl
Innerchr14:35806100..35842300hg18UCSC Ensembl
Innerchr14:35806100..35842300hg17UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3836201
hg1936201
hg1836201
hg1736201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34543
Supporting Variants
SamplesNA10830
Known GenesMBIP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987067
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