A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626656



Internal ID7013488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64018433..64019361hg38UCSC Ensembl
Innerchr11:64018433..64019361hg38UCSC Ensembl
Outerchr11:64018075..64019686hg38UCSC Ensembl
chr11:63785905..63786833hg19UCSC Ensembl
Innerchr11:63785905..63786833hg19UCSC Ensembl
Outerchr11:63785547..63787158hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14184918, essv14184915, essv14184919, essv14184916, essv14184917, essv14184924, essv14184925, essv14184923, essv14184921, essv14184922, essv14184920, essv14184914
SamplesHG03800, HG01795, HG02360, HG03805, HG03823, NA19000, NA18555, NA18536, NA18615, NA19078, HG00513, HG01912
Known GenesMACROD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626656
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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