A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14326932



Internal ID4277859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134933906..135024674hg38UCSC Ensembl
Innerchr11:134934056..135024524hg38UCSC Ensembl
Outerchr11:134933756..135024824hg38UCSC Ensembl
chr11:134803800..134894568hg19UCSC Ensembl
Innerchr11:134803950..134894418hg19UCSC Ensembl
Outerchr11:134803650..134894718hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3890769
hg1990769
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628204
Supporting Variants
SamplesHG03844
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14326932
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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