A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989265



Internal ID12974016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93610311..93693179hg38UCSC Ensembl
Innerchr15:94153540..94236408hg19UCSC Ensembl
Innerchr15:91954544..92037412hg18UCSC Ensembl
Innerchr15:91954544..92037412hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3882869
hg1982869
hg1882869
hg1782869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751543
Supporting Variants
SamplesBEC_492
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989265
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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