A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627962



Internal ID7014787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123706983..123724583hg38UCSC Ensembl
chr11:123577691..123595291hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3817601
hg1917601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14301314, essv14301315, essv14301309, essv14301312, essv14301310, essv14301316, essv14301313, essv14301311
SamplesHG02040, HG01341, NA18940, NA19728, HG01369, NA18987, HG02348, HG02778
Known GenesZNF202
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627962
Frequency
Sample Size2504
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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