A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612444



Internal ID6999345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18047621..18074078hg38UCSC Ensembl
chr7:18087244..18113701hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3826458
hg1926458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12691078
SamplesHG03991
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612444
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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