A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613738



Internal ID6653946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75775011..75778869hg38UCSC Ensembl
Innerchr7:75775025..75778855hg38UCSC Ensembl
Outerchr7:75774997..75778883hg38UCSC Ensembl
chr7:75404329..75408187hg19UCSC Ensembl
Innerchr7:75404343..75408173hg19UCSC Ensembl
Outerchr7:75404315..75408201hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383859
hg193859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12848221
SamplesHG02095
Known GenesCCL26
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613738
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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