A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990316



Internal ID12632808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100977272..101032172hg38UCSC Ensembl
Innerchr15:101517477..101572377hg19UCSC Ensembl
Innerchr15:99335000..99389900hg18UCSC Ensembl
Innerchr15:99335000..99389900hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3854901
hg1954901
hg1854901
hg1754901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34275
Supporting Variants
SamplesNA12815
Known GenesLRRK1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990316
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