A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625996



Internal ID7012830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37930227..38067759hg38UCSC Ensembl
Innerchr11:37930261..38067726hg38UCSC Ensembl
Outerchr11:37930194..38067793hg38UCSC Ensembl
chr11:37951777..38089309hg19UCSC Ensembl
Innerchr11:37951811..38089276hg19UCSC Ensembl
Outerchr11:37951744..38089343hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38137533
hg19137533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14095035
SamplesHG03782
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625996
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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