A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614200



Internal ID7001095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95707754..95735519hg38UCSC Ensembl
chr7:95337066..95364831hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3827766
hg1927766
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1313e214
Supporting Variantsessv12900850, essv12900846, essv12900848, essv12900847, essv12900852, essv12900849, essv12900854, essv12900855, essv12900851, essv12900856, essv12900853
SamplesHG01860, HG00560, HG02142, HG00533, HG00956, HG00690, HG01842, NA18608, HG02179, HG01862, HG02353
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614200
Frequency
Sample Size2504
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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