A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983295



Internal ID12976071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9556956..9660955hg38UCSC Ensembl
Innerchr16:9650813..9754812hg19UCSC Ensembl
Innerchr16:9558314..9662313hg18UCSC Ensembl
Innerchr16:9558314..9662313hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38104000
hg19104000
hg18104000
hg17104000
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751617
Supporting Variants
SamplesBEC_636
Known GenesMIR7641-2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983295
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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