A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988101



Internal ID12632951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82614804..82784743hg38UCSC Ensembl
Innerchr15:83283555..83453495hg19UCSC Ensembl
Innerchr15:81080610..81250549hg18UCSC Ensembl
Innerchr15:81080610..81250549hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38169940
hg19169941
hg18169940
hg17169940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34318
Supporting Variants
SamplesNA12891
Known GenesAP3B2, CPEB1, FSD2, LOC283692, LOC283693, LOC338963, SCARNA15
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988101
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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