A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987424



Internal ID12629272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27525878..27701078hg38UCSC Ensembl
Innerchr16:27537199..27712399hg19UCSC Ensembl
Innerchr16:27444700..27619900hg18UCSC Ensembl
Innerchr16:27444700..27619900hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38175201
hg19175201
hg18175201
hg17175201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751555
Supporting Variants
SamplesBEC_629
Known GenesGTF3C1, KIAA0556
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987424
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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