A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585062



Internal ID6625380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:4203541..4292960hg38UCSC Ensembl
chr1:4263601..4353020hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3889420
hg1989420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9844493
SamplesHG02481
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585062
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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