A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600668



Internal ID6987709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:60409562..60495202hg38UCSC Ensembl
chr4:61275280..61360920hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3885641
hg1985641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11447708, essv11447710, essv11447707, essv11447711, essv11447713, essv11447712, essv11447705, essv11447709, essv11447706
SamplesHG03821, NA21109, HG04047, NA21119, HG04235, HG03858, NA20872, HG03729, NA21088
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600668
Frequency
Sample Size2504
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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