A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979095



Internal ID12632938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82627794..82771594hg38UCSC Ensembl
Innerchr15:83296545..83440346hg19UCSC Ensembl
Innerchr15:81093600..81237400hg18UCSC Ensembl
Innerchr15:81093600..81237400hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38143801
hg19143802
hg18143801
hg17143801
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)essv6979095
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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