A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657728



Internal ID9923833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16643503..16643961hg38UCSC Ensembl
chr7:16683128..16683586hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5690428, essv5948993, essv6177516, essv6085343, essv5531039, essv6299530, essv5837657, essv5410956, essv6501343, essv6283669, essv5958015, essv5743793, essv5799452, essv6213880, essv6163949, essv6453750, essv5458825, essv5921285, essv5820725, essv5740527
SamplesHG01441, NA18508, NA19704, NA19319, NA19457, NA20287, NA19384, NA19372, NA19371, NA19385, NA19236, NA19452, NA19318, NA19395, NA19440, NA19380, NA19428, NA18501, NA19093, NA19431
Known GenesANKMY2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657728
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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