A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978323



Internal ID12635103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51063711..51460611hg38UCSC Ensembl
Innerchr15:51355908..51752808hg19UCSC Ensembl
Innerchr15:49143200..49540100hg18UCSC Ensembl
Innerchr15:49143200..49540100hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38396901
hg19396901
hg18396901
hg17396901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34532
Supporting Variants
SamplesNA19000
Known GenesCYP19A1, DMXL2, GLDN, MIR4713, TNFAIP8L3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978323
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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