A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987327



Internal ID12631971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21843979..22889617hg38UCSC Ensembl
Innerchr19:22026781..23072419hg19UCSC Ensembl
Innerchr19:21818621..22864259hg18UCSC Ensembl
Innerchr19:21818621..22864259hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381045639
hg191045639
hg181045639
hg171045639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34340
Supporting Variants
SamplesNA11839
Known GenesLOC100996349, LOC440518, ZNF208, ZNF257, ZNF43, ZNF492, ZNF676, ZNF729, ZNF98, ZNF99
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987327
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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