A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979017



Internal ID12632812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100977282..101049435hg38UCSC Ensembl
Innerchr15:101517487..101589640hg19UCSC Ensembl
Innerchr15:99335010..99407163hg18UCSC Ensembl
Innerchr15:99335010..99407163hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3872154
hg1972154
hg1872154
hg1772154
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)essv6979017
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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