A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979212



Internal ID12979805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:56392010..56601610hg38UCSC Ensembl
Innerchr15:56684208..56893808hg19UCSC Ensembl
Innerchr15:54471500..54681100hg18UCSC Ensembl
Innerchr15:54471500..54681100hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38209601
hg19209601
hg18209601
hg17209601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35150
Supporting Variants
SamplesNA18507
Known GenesMNS1, TEX9
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979212
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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