A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892612



Internal ID19183432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:21131239..22303801hg38UCSC Ensembl
Outerchr15:21336568..22591752hg19UCSC Ensembl
Innerchr15:19633950..20016954hg18UCSC Ensembl
Outerchr15:19601227..20093116hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381172563
hg191255185
hg18491890
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791463, essv25791979, essv25791967, essv25790935, essv25790487, essv25791518
Samples
Known GenesCXADRP2, LOC646214, LOC727924, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892612
Frequency
Sample Size3017
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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