A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603211



Internal ID6990243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173488228..173492431hg38UCSC Ensembl
Innerchr4:173488271..173492389hg38UCSC Ensembl
Outerchr4:173488186..173492474hg38UCSC Ensembl
chr4:174409379..174413582hg19UCSC Ensembl
Innerchr4:174409422..174413540hg19UCSC Ensembl
Outerchr4:174409337..174413625hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg384204
hg194204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11707407, essv11707404, essv11707405, essv11707406
SamplesHG03514, HG00306, HG02941, HG03442
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603211
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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