A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603096



Internal ID6643351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168155186..168157931hg38UCSC Ensembl
Innerchr4:168155248..168157870hg38UCSC Ensembl
Outerchr4:168155125..168157993hg38UCSC Ensembl
chr4:169076337..169079082hg19UCSC Ensembl
Innerchr4:169076399..169079021hg19UCSC Ensembl
Outerchr4:169076276..169079144hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382746
hg192746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11686649
SamplesHG01679
Known GenesANXA10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603096
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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