A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615169



Internal ID7002058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137475589..137541006hg38UCSC Ensembl
chr7:137160335..137225752hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3865418
hg1965418
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12979597
SamplesHG01365
Known GenesDGKI
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615169
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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