A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14034665



Internal ID4007212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15536712..15544562hg38UCSC Ensembl
Innerchr11:15537212..15544062hg38UCSC Ensembl
Outerchr11:15535712..15545562hg38UCSC Ensembl
chr11:15558258..15566108hg19UCSC Ensembl
Innerchr11:15558758..15565608hg19UCSC Ensembl
Outerchr11:15557258..15567108hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg387851
hg197851
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625438
Supporting Variants
SamplesHG03660
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14034665
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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