A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585271



Internal ID6972796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13986481..14046537hg38UCSC Ensembl
chr1:14312976..14373032hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3860057
hg1960057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8e214
Supporting Variantsessv9860532, essv9860531
SamplesNA18861, HG03130
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585271
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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