A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983618



Internal ID12976589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20662464..22300068hg38UCSC Ensembl
Innerchr15:20867793..22588019hg19UCSC Ensembl
Innerchr15:19127807..20089383hg18UCSC Ensembl
Innerchr15:19127807..20089383hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381637605
hg191720227
hg18961577
hg17961577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751468
Supporting Variants
SamplesBEC_673
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)essv6983618
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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