A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625133



Internal ID7011971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3044640..3045534hg38UCSC Ensembl
Innerchr11:3044640..3045534hg38UCSC Ensembl
Outerchr11:3044320..3045831hg38UCSC Ensembl
chr11:3065870..3066764hg19UCSC Ensembl
Innerchr11:3065870..3066764hg19UCSC Ensembl
Outerchr11:3065550..3067061hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38895
hg19895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13993635, essv13993634, essv13993642, essv13993633, essv13993632, essv13993637, essv13993638, essv13993640, essv13993641, essv13993639, essv13993636
SamplesHG01885, HG00187, HG00369, HG03114, NA19175, HG00428, HG02976, HG00276, NA19108, HG00357, HG00345
Known GenesCARS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625133
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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