A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981132



Internal ID12626169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6961171..6997362hg38UCSC Ensembl
Innerchr19:6961182..6997373hg19UCSC Ensembl
Innerchr19:6912182..6948373hg18UCSC Ensembl
Innerchr19:6912182..6948373hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3836192
hg1936192
hg1836192
hg1736192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751810
Supporting Variants
SamplesBEC_355
Known GenesEMR4P
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981132
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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