A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34892



Internal ID12644242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90104756..90235264hg38UCSC Ensembl
Innerchr15:90647988..90778496hg19UCSC Ensembl
Innerchr15:88448992..88579500hg18UCSC Ensembl
Innerchr15:88448992..88579500hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38130509
hg19130509
hg18130509
hg17130509
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv112e55
Supporting Variantsessv6980556, essv6986020, essv6990496
SamplesNA19209
Known GenesCIB1, GDPGP1, SEMA4B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34892
Frequency
Sample Size771
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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