A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6489188



Internal ID9466591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21958734..22958455hg38UCSC Ensembl
chr19:22141536..23141257hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38999722
hg19999722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660015
Supporting Variants
SamplesNA18964
Known GenesLOC100996349, LOC440518, ZNF208, ZNF257, ZNF492, ZNF676, ZNF729, ZNF98, ZNF99
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6489188
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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