A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988126



Internal ID12979811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:56392004..56601616hg38UCSC Ensembl
Innerchr15:56684202..56893814hg19UCSC Ensembl
Innerchr15:54471494..54681106hg18UCSC Ensembl
Innerchr15:54471494..54681106hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38209613
hg19209613
hg18209613
hg17209613
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)essv6988126
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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