A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612073



Internal ID6998975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7288774..7395834hg38UCSC Ensembl
chr7:7328405..7435465hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38107061
hg19107061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12674624, essv12674622, essv12674623, essv12674625
SamplesHG02973, NA19099, HG02255, HG03401
Known GenesCOL28A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612073
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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