A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983884



Internal ID12630645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34637550..34692790hg38UCSC Ensembl
Innerchr15:34929751..34984991hg19UCSC Ensembl
Innerchr15:32717043..32772283hg18UCSC Ensembl
Innerchr15:32717043..32772283hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3855241
hg1955241
hg1855241
hg1755241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751533
Supporting Variants
SamplesBEC_728
Known GenesMIR5588
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983884
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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