A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986027



Internal ID12635971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90109624..90235254hg38UCSC Ensembl
Innerchr15:90652856..90778486hg19UCSC Ensembl
Innerchr15:88453860..88579490hg18UCSC Ensembl
Innerchr15:88453860..88579490hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38125631
hg19125631
hg18125631
hg17125631
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34510
Supporting Variants
SamplesNA19211
Known GenesCIB1, GDPGP1, SEMA4B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986027
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