A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660015



Internal ID9579434
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 Flag
Merged StatusM
Merged Variantsdgv633e199
Supporting Variantsessv5500793, essv6458579, essv6549748, essv5776719, essv5423202, essv6489188, essv5610722, essv6446281, essv5934947
SamplesNA18870, HG01492, NA18964, NA19372, HG00464, NA19007, HG01047, NA20504, NA18511
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)esv2660015
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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