A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv633e199



Internal ID20123935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21927913..23001069hg38UCSC Ensembl
chr19:22110715..23183871hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381073157
hg191073157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2664371, esv2669125, esv2671513, esv2660015
SamplesNA19909, HG00384, NA18565, HG00306, NA19057, NA18616, NA18870, NA18567, NA18619, HG01492, NA18618, NA12283, NA18498, NA18964, NA19130, NA18949, NA18611, NA18874, NA19372, HG01440, NA19901, NA20755, HG00464, NA19007, NA20800, HG00266, NA19236, HG00740, HG01047, HG01383, NA12827, NA18945, HG00155, NA19434, NA20504, NA20803, HG01342, NA06986, NA20807, NA20758, NA19463, NA18511, NA18622, NA18965, NA18577
Known GenesLOC100996349, LOC440518, ZNF208, ZNF257, ZNF492, ZNF676, ZNF728, ZNF729, ZNF98, ZNF99
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv633e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss45
Observed Complex0
Frequencyn/a


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