A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615213



Internal ID7002102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139493880..139508650hg38UCSC Ensembl
chr7:139178626..139193396hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3814771
hg1914771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12982063
SamplesNA19732
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615213
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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