A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv203e214



Internal ID20121626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62504574..62530771hg38UCSC Ensembl
chr11:62272046..62298243hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3826198
hg1926198
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3626610, esv3626611
SamplesHG00142, HG00610, HG00190, HG02896, HG02721
Known GenesAHNAK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv203e214
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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