A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9839472



Internal ID5253937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:837710..917284hg38UCSC Ensembl
chr1:773090..852664hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3879575
hg1979575
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3584982
Supporting Variants
SamplesNA18635
Known GenesFAM41C, LINC01128
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9839472
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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