A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615689



Internal ID7002578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157297091..157320276hg38UCSC Ensembl
chr7:157089785..157112970hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3823186
hg1923186
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13040095, essv13040096
SamplesHG03132, NA19338
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615689
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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