A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615244



Internal ID7002133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140890999..140905323hg38UCSC Ensembl
Innerchr7:140891149..140905173hg38UCSC Ensembl
Outerchr7:140890849..140905473hg38UCSC Ensembl
chr7:140590799..140605123hg19UCSC Ensembl
Innerchr7:140590949..140604973hg19UCSC Ensembl
Outerchr7:140590649..140605273hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3814325
hg1914325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12985094
SamplesHG04235
Known GenesBRAF
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615244
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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