A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672319



Internal ID9591738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35360914..35372220hg38UCSC Ensembl
Outerchr19:35360543..35372590hg38UCSC Ensembl
Innerchr19:35851816..35863122hg19UCSC Ensembl
Outerchr19:35851445..35863492hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812048
hg1912048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv637e199
Supporting Variantsessv6494172, essv6242657, essv5774824, essv5693968, essv6589507, essv6100780, essv6376173, essv5787455, essv6386818, essv6105427, essv6574478, essv5903517, essv5945614, essv5772624, essv5976726, essv5866575, essv6123549, essv6385397, essv5437748, essv6069976, essv5617564, essv6493921, essv6504319, essv5801027, essv5672484, essv6385483, essv6084218, essv6539110, essv6127786, essv6090836, essv6178015, essv6013376, essv5617964, essv5861174, essv5646000, essv6014138, essv6025872
SamplesNA18621, NA18595, NA18534, NA18530, NA18630, NA18612, NA18570, NA18545, NA18573, NA18608, NA18541, NA18632, NA18624, NA18635, NA18576, NA18563, NA18618, NA18636, NA18638, NA18547, NA18593, NA18539, NA18564, NA18562, NA18579, NA18543, NA18619, NA18582, NA18597, NA18599, NA18538, NA18565, NA18631, NA18560, NA18610, NA18532, NA18555
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672319
Frequency
Sample Size1151
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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