A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982057



Internal ID12627692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4120408..4238918hg38UCSC Ensembl
Innerchr16:4170409..4288919hg19UCSC Ensembl
Innerchr16:4110410..4228920hg18UCSC Ensembl
Innerchr16:4110410..4228920hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38118511
hg19118511
hg18118511
hg17118511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751608
Supporting Variants
SamplesBEC_516
Known GenesSRL
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982057
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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