A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989884



Internal ID12977435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21284651..21543535hg38UCSC Ensembl
Innerchr19:21467453..21726337hg19UCSC Ensembl
Innerchr19:21259293..21518177hg18UCSC Ensembl
Innerchr19:21259293..21518177hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38258885
hg19258885
hg18258885
hg17258885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751783
Supporting Variants
SamplesBEC_737
Known GenesLINC00664, ZNF429, ZNF493, ZNF708, ZNF738
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989884
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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