A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657153



Internal ID9576572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3627786..3630092hg38UCSC Ensembl
Outerchr11:3627415..3630462hg38UCSC Ensembl
Innerchr11:3649016..3651322hg19UCSC Ensembl
Outerchr11:3648645..3651692hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383048
hg193048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv186e199
Supporting Variantsessv6206910, essv6190474, essv5731242, essv5856743, essv5786647, essv6202114, essv6220110, essv5797086, essv6109635, essv5423656, essv5848530, essv6080997, essv5809733, essv6546957, essv5507810, essv6331783, essv5691599, essv5423175, essv5914200, essv5594549, essv6358518, essv5723886, essv5469068, essv6336434, essv5818865, essv6213775, essv6358179, essv6223473, essv6412278, essv5869264, essv5439524, essv6351306, essv5798356, essv6518169, essv6431214, essv5957530, essv5845304
SamplesHG00626, HG00403, HG00650, HG00542, HG00592, HG00608, HG00671, HG00699, HG00534, HG00427, HG00419, HG00464, HG00543, HG00560, HG00629, HG00443, HG00653, HG00577, HG00475, HG00436, HG00533, HG00708, HG00692, HG00651, HG00690, HG00531, HG00613, HG00463, HG00611, HG00476, HG00580, HG00607, HG00620, HG00707, HG00578, HG00478, HG00472
Known GenesTRPC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657153
Frequency
Sample Size1151
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer