A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1349e199



Internal ID22759122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62601544..62607391hg38UCSC Ensembl
chr9:46912845..46918692hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385848
hg195848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2662190, esv2676525
SamplesHG00593, HG00626, HG00403, HG01441, HG00650, HG00542, HG00536, HG00608, HG01359, HG01465, HG00449, HG00663, HG00589, HG00501, HG01488, HG00702, HG00689, HG00610, HG01354, HG01365, HG00512, HG01495, HG00422, HG00705, HG01550, HG00530, HG00419, HG01124, HG01353, HG00543, HG01136, HG00560, HG00629, HG00443, HG01360, HG01384, HG00557, HG00428, HG00653, HG00701, HG00475, HG00556, HG00583, HG01498, HG01149, HG00619, HG00692, HG00651, HG00404, HG00531, HG00479, HG00684, HG01383, HG00525, HG01497, HG00704, HG00463, HG01148, HG00611, HG00476, HG00565, HG01551, HG01375, HG00473, HG01494, HG00607, HG01113, HG01137, HG00662, HG00418, HG01489, HG01342, HG00707, HG00614, HG00513, HG00478, HG00421, HG00656, HG01254, HG00472, HG00628, HG01112, HG01437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1349e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss83
Observed Complex0
Frequencyn/a


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