A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986017



Internal ID12635919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20646884..22300085hg38UCSC Ensembl
Innerchr15:20852186..22588036hg19UCSC Ensembl
Innerchr15:19112200..20089400hg18UCSC Ensembl
Innerchr15:19112200..20089400hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381653202
hg191735851
hg18977201
hg17977201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34827
Supporting Variants
SamplesNA19208
Known GenesCT60, CXADRP2, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986017
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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