A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625533



Internal ID6665681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19202187..19202876hg38UCSC Ensembl
Innerchr11:19202192..19202871hg38UCSC Ensembl
Outerchr11:19202182..19202881hg38UCSC Ensembl
chr11:19223734..19224423hg19UCSC Ensembl
Innerchr11:19223739..19224418hg19UCSC Ensembl
Outerchr11:19223729..19224428hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14045330
SamplesHG04195
Known GenesCSRP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625533
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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