A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625945



Internal ID7012779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36063935..36085148hg38UCSC Ensembl
Innerchr11:36063940..36085143hg38UCSC Ensembl
Outerchr11:36063930..36085153hg38UCSC Ensembl
chr11:36085485..36106698hg19UCSC Ensembl
Innerchr11:36085490..36106693hg19UCSC Ensembl
Outerchr11:36085480..36106703hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3821214
hg1921214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv190e214
Supporting Variantsessv14090626
SamplesHG03928
Known GenesLDLRAD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625945
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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