A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986771



Internal ID12632815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100977282..101482551hg38UCSC Ensembl
Innerchr15:101517487..102022756hg19UCSC Ensembl
Innerchr15:99335010..99840279hg18UCSC Ensembl
Innerchr15:99335010..99840279hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38505270
hg19505270
hg18505270
hg17505270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34275
Supporting Variants
SamplesNA12815
Known GenesCHSY1, LOC100507472, LRRK1, PCSK6, SNRPA1, VIMP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986771
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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