A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661548



Internal ID9927653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15915626..15919699hg38UCSC Ensembl
chr19:16026436..16030509hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg384074
hg194074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6377910, essv5462418, essv6070358, essv5899729, essv5398776, essv6147492, essv5476215, essv5694418, essv6276285, essv5929976
SamplesNA18980, HG00634, NA19062, NA18574, HG00543, NA18613, NA18535, NA18952, HG00707, NA18989
Known GenesCYP4F11
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661548
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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