A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987359



Internal ID12981685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20908541..22270557hg38UCSC Ensembl
Innerchr15:21113870..22558508hg19UCSC Ensembl
Innerchr15:19378495..20059872hg18UCSC Ensembl
Innerchr15:19378495..20059872hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381362017
hg191444639
hg18681378
hg17681378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35107
Supporting Variants
SamplesNA18994
Known GenesCT60, CXADRP2, LOC646214, LOC727924, 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)essv6987359
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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