A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625327



Internal ID7012161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9234005..9236399hg38UCSC Ensembl
Innerchr11:9234055..9236349hg38UCSC Ensembl
Outerchr11:9233955..9236449hg38UCSC Ensembl
chr11:9255552..9257946hg19UCSC Ensembl
Innerchr11:9255602..9257896hg19UCSC Ensembl
Outerchr11:9255502..9257996hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382395
hg192395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14021556
SamplesHG03049
Known GenesDENND5A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625327
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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