A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625870



Internal ID7012704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33023135..33034479hg38UCSC Ensembl
Innerchr11:33023135..33034479hg38UCSC Ensembl
Outerchr11:33022890..33034742hg38UCSC Ensembl
chr11:33044681..33056025hg19UCSC Ensembl
Innerchr11:33044681..33056025hg19UCSC Ensembl
Outerchr11:33044436..33056288hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3811345
hg1911345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14085170, essv14085169
SamplesHG01372, HG01257
Known GenesDEPDC7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625870
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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