A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978111



Internal ID12631968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22028658..22535758hg38UCSC Ensembl
Innerchr19:22211460..22718560hg19UCSC Ensembl
Innerchr19:22003300..22510400hg18UCSC Ensembl
Innerchr19:22003300..22510400hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38507101
hg19507101
hg18507101
hg17507101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34340
Supporting Variants
SamplesNA11839
Known GenesZNF257, ZNF676, ZNF729, ZNF98
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978111
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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