A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613688



Internal ID7000584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73640677..73653193hg38UCSC Ensembl
chr7:73055007..73067523hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3812517
hg1912517
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12841054
SamplesNA19332
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613688
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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