A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979920



Internal ID12634280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669805..15714929hg38UCSC Ensembl
Innerchr19:15780615..15825739hg19UCSC Ensembl
Innerchr19:15641615..15686739hg18UCSC Ensembl
Innerchr19:15641615..15686739hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3845125
hg1945125
hg1845125
hg1745125
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34334
Supporting Variants
SamplesNA18860
Known GenesCYP4F12
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979920
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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