A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612779



Internal ID6999679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:33861781..33942872hg38UCSC Ensembl
chr7:33901393..33982484hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3881092
hg1981092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12723743
SamplesHG00446
Known GenesBMPER
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612779
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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