A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626638



Internal ID7013470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63418984..63432304hg38UCSC Ensembl
chr11:63186456..63199776hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3813321
hg1913321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv205e214
Supporting Variantsessv14183607, essv14183615, essv14183606, essv14183592, essv14183593, essv14183603, essv14183611, essv14183588, essv14183590, essv14183617, essv14183605, essv14183613, essv14183600, essv14183591, essv14183602, essv14183589, essv14183595, essv14183594, essv14183616, essv14183601, essv14183618, essv14183599, essv14183610, essv14183608, essv14183609, essv14183598, essv14183614, essv14183596, essv14183597, essv14183604, essv14183612
SamplesHG00881, NA21111, HG00457, HG04002, NA19446, NA18574, HG02395, HG01950, HG00406, NA18640, HG00675, NA18645, NA18747, HG00982, HG00428, HG01498, HG04019, HG01852, HG00844, HG02884, HG00525, HG01865, HG03437, NA19735, HG03084, HG01432, HG02367, NA18636, NA18740, NA18562, HG00593
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626638
Frequency
Sample Size2504
Observed Gain31
Observed Loss0
Observed Complex0
Frequencyn/a


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