A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660204



Internal ID2893291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45310891..45311354hg38UCSC Ensembl
chr19:45814149..45814612hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6424071, essv6035042, essv6565407, essv5668916, essv5901362, essv6019930, essv6106041, essv5728876, essv5630949, essv5750599
SamplesNA19449, HG01551, NA19428, NA18934, NA19313, NA19318, NA19235, NA19446, NA19371, NA19130
Known GenesCKM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660204
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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