A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979211



Internal ID12979806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:56392004..56604106hg38UCSC Ensembl
Innerchr15:56684202..56896304hg19UCSC Ensembl
Innerchr15:54471494..54683596hg18UCSC Ensembl
Innerchr15:54471494..54683596hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38212103
hg19212103
hg18212103
hg17212103
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)essv6979211
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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