A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602124



Internal ID6989158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:126466126..126532584hg38UCSC Ensembl
Innerchr4:126466126..126532584hg38UCSC Ensembl
Outerchr4:126465626..126533084hg38UCSC Ensembl
chr4:127387281..127453739hg19UCSC Ensembl
Innerchr4:127387281..127453739hg19UCSC Ensembl
Outerchr4:127386781..127454239hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3866459
hg1966459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11595795
SamplesHG01859
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602124
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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