A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985663



Internal ID12625944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20778925..22300068hg38UCSC Ensembl
Innerchr15:20984254..22588019hg19UCSC Ensembl
Innerchr15:19244303..20089383hg18UCSC Ensembl
Innerchr15:19244303..20089383hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381521144
hg191603766
hg18845081
hg17845081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751358
Supporting Variants
SamplesBEC_333
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)essv6985663
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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