A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614116



Internal ID7001011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91078859..91104331hg38UCSC Ensembl
Innerchr7:91078859..91104331hg38UCSC Ensembl
Outerchr7:91078359..91104831hg38UCSC Ensembl
chr7:90708174..90733646hg19UCSC Ensembl
Innerchr7:90708174..90733646hg19UCSC Ensembl
Outerchr7:90707674..90734146hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3825473
hg1925473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12886944
SamplesNA20884
Known GenesCDK14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614116
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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