A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603130



Internal ID6990162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169877462..169882167hg38UCSC Ensembl
Innerchr4:169877472..169882157hg38UCSC Ensembl
Outerchr4:169877452..169882177hg38UCSC Ensembl
chr4:170798613..170803318hg19UCSC Ensembl
Innerchr4:170798623..170803308hg19UCSC Ensembl
Outerchr4:170798603..170803328hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg384706
hg194706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11690424, essv11690425, essv11690426, essv11690423
SamplesHG02571, HG02953, HG01049, NA18865
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603130
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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