A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612822



Internal ID6653035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35882383..35953804hg38UCSC Ensembl
chr7:35921993..35993414hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3871422
hg1971422
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12732356, essv12732358, essv12732354, essv12732355, essv12732357, essv12732353
SamplesHG02470, HG03380, HG03193, HG03195, HG03428, NA19131
Known GenesSEPT7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612822
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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