A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981964



Internal ID12627552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33661649..35887724hg38UCSC Ensembl
Innerchr16:33464116..35122095hg19UCSC Ensembl
Innerchr16:33371617..34979596hg18UCSC Ensembl
Innerchr16:33371617..34979596hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg382226076
hg191657980
hg181607980
hg171607980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751556
Supporting Variants
SamplesBEC_51
Known GenesFLJ26245, LINC00273, LOC100130700, LOC146481, LOC283914, RNU6-76P, UBE2MP1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981964
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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