A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585272



Internal ID6972797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13988964..14044277hg38UCSC Ensembl
chr1:14315459..14370772hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3855314
hg1955314
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8e214
Supporting Variantsessv9860534, essv9860533, essv9860535
SamplesNA18861, HG03130, NA18618
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585272
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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