A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9853732



Internal ID1315443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11389777..11476160hg38UCSC Ensembl
chr1:11449834..11536217hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3886384
hg1986384
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585221
Supporting Variants
SamplesHG01162
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9853732
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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