A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980995



Internal ID12635720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15686590..15714890hg38UCSC Ensembl
Innerchr19:15797400..15825700hg19UCSC Ensembl
Innerchr19:15658400..15686700hg18UCSC Ensembl
Innerchr19:15658400..15686700hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3828301
hg1928301
hg1828301
hg1728301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35069
Supporting Variants
SamplesNA19171
Known GenesCYP4F12
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980995
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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