A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751542



Internal ID12985094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92510451..92548585hg38UCSC Ensembl
Innerchr15:93053681..93091815hg19UCSC Ensembl
Innerchr15:90854685..90892819hg18UCSC Ensembl
Innerchr15:90854685..90892819hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3838135
hg1938135
hg1838135
hg1738135
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6986386, essv6983262
SamplesBEC_560
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751542
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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