A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983297



Internal ID12976069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9560112..9646682hg38UCSC Ensembl
Innerchr16:9653969..9740539hg19UCSC Ensembl
Innerchr16:9561470..9648040hg18UCSC Ensembl
Innerchr16:9561470..9648040hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3886571
hg1986571
hg1886571
hg1786571
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983297
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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