A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3584981



Internal ID6972505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:837710..917284hg38UCSC Ensembl
chr1:773090..852664hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3879575
hg1979575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9839424, essv9839425
SamplesHG00743, HG01444
Known GenesFAM41C, LINC01128
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3584981
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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