A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625152



Internal ID7011990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3630637..3640995hg38UCSC Ensembl
Innerchr11:3630787..3640845hg38UCSC Ensembl
Outerchr11:3630487..3641145hg38UCSC Ensembl
chr11:3651867..3662225hg19UCSC Ensembl
Innerchr11:3652017..3662075hg19UCSC Ensembl
Outerchr11:3651717..3662375hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3810359
hg1910359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13997026
SamplesHG00707
Known GenesART5, TRPC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625152
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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