A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv623e199



Internal ID18982677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11928230..11935777hg38UCSC Ensembl
chr19:12039045..12046592hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387548
hg197548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2678865, esv2666815
SamplesNA19207, NA18870, NA19248, NA19445, NA19625, NA18520, NA19321, HG01052, NA18933, NA19404, NA19437, NA19114, NA18874, NA19093, NA19223, NA19455, NA19319, NA19430, NA18516, NA19317, NA19334, NA19451, NA18517, NA18489, NA19461, NA19257, HG00578, NA19108, NA19355, NA19472, NA19467, NA19147, NA19438, HG00635, NA19463, HG01148, NA19428, NA19383, NA18934, NA19390, HG00638, NA18856, NA19429, NA19256, NA18916, NA19457, NA19324, NA19247, NA19360, NA19313, NA19129, NA19172, NA19189, NA19372, NA19393, NA19373, NA19384, NA18923, NA19102, NA18522, NA18502, NA19119, NA19098, NA18858, NA19347, NA19332, NA19131, NA19159, NA18910, NA19235, NA19376, NA18907, NA19391, NA19394, NA19403, NA19116, NA19434, NA19818, NA19099, NA19446, NA19225, NA12546, NA19160, NA19371, NA19198, NA19470, NA19315, NA19346, NA18853, HG01489, NA19473, NA19468, NA19456, NA19466, HG01198
Known GenesZNF700
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv623e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss95
Observed Complex0
Frequencyn/a


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