A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989396



Internal ID12977314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28184553..28262453hg38UCSC Ensembl
Innerchr19:28675460..28753360hg19UCSC Ensembl
Innerchr19:33367300..33445200hg18UCSC Ensembl
Innerchr19:33367300..33445200hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3877901
hg1977901
hg1877901
hg1777901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751785
Supporting Variants
SamplesBEC_727
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989396
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer