A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978109



Internal ID12631966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21889431..22889617hg38UCSC Ensembl
Innerchr19:22072233..23072419hg19UCSC Ensembl
Innerchr19:21864073..22864259hg18UCSC Ensembl
Innerchr19:21864073..22864259hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381000187
hg191000187
hg181000187
hg171000187
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, ZNF492, ZNF676, ZNF729, ZNF98, ZNF99
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978109
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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