A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987791



Internal ID12982418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24832797..24833868hg38UCSC Ensembl
Innerchr15:25077944..25079015hg19UCSC Ensembl
Innerchr15:22629037..22630108hg18UCSC Ensembl
Innerchr15:22629037..22630108hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381072
hg191072
hg181072
hg171072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34441
Supporting Variants
SamplesNA19172
Known GenesSNRPN
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987791
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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