A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979210



Internal ID12979807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:56385532..56604106hg38UCSC Ensembl
Innerchr15:56677730..56896304hg19UCSC Ensembl
Innerchr15:54465022..54683596hg18UCSC Ensembl
Innerchr15:54465022..54683596hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38218575
hg19218575
hg18218575
hg17218575
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979210
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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