A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671286



Internal ID9937391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107365290..107374096hg38UCSC Ensembl
Outerchr11:107364919..107374466hg38UCSC Ensembl
Innerchr11:107236016..107244822hg19UCSC Ensembl
Outerchr11:107235645..107245192hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg389548
hg199548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv239e199
Supporting Variantsessv5867730, essv5736902, essv5843305, essv5688370, essv5539873, essv6538202, essv6170004, essv5851210, essv5811033, essv6388000, essv6553723, essv6324056, essv6369789, essv5790099, essv6392681, essv6485109, essv5730188, essv5743424, essv6178047, essv6591086, essv5847908, essv5936620, essv6564511, essv5572700, essv5891645, essv6090802, essv6212056, essv5612505, essv6405174, essv5623996, essv6499486, essv5832074, essv6583795, essv6332900
SamplesHG00650, HG00608, HG00693, HG00663, HG00702, HG00448, HG00610, HG00590, HG00683, HG00543, HG00560, HG00443, HG00701, HG00657, HG00533, HG00583, HG00500, HG00619, HG00635, HG00690, HG00404, HG00531, HG00684, HG00613, HG00525, HG00463, HG00611, HG00476, HG00580, HG00473, HG00418, HG00614, HG00698, HG00593
Known GenesCWF19L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671286
Frequency
Sample Size1151
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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