A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615056



Internal ID7001945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132637109..132654399hg38UCSC Ensembl
chr7:132321868..132339158hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3817291
hg1917291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12973520
SamplesNA19684
Known GenesFLJ40288, PLXNA4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615056
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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