A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987217



Internal ID12983139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85287462..85569198hg38UCSC Ensembl
Innerchr15:85830693..86112429hg19UCSC Ensembl
Innerchr15:83631697..83913433hg18UCSC Ensembl
Innerchr15:83631697..83913433hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38281737
hg19281737
hg18281737
hg17281737
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751538
Supporting Variants
SamplesSPC_141
Known GenesAKAP13
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987217
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