A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603142



Internal ID6990174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170364178..170452829hg38UCSC Ensembl
Innerchr4:170364178..170452829hg38UCSC Ensembl
Outerchr4:170363678..170453329hg38UCSC Ensembl
chr4:171285329..171373980hg19UCSC Ensembl
Innerchr4:171285329..171373980hg19UCSC Ensembl
Outerchr4:171284829..171374480hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3888652
hg1988652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11693800
SamplesHG02009
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603142
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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