A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982180



Internal ID12973315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87219818..87326577hg38UCSC Ensembl
Innerchr15:87763049..87869808hg19UCSC Ensembl
Innerchr15:85564053..85670812hg18UCSC Ensembl
Innerchr15:85564053..85670812hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38106760
hg19106760
hg18106760
hg17106760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751539
Supporting Variants
SamplesBEC_400
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982180
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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