A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611943



Internal ID6998845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4654295..4663117hg38UCSC Ensembl
Innerchr7:4654795..4662617hg38UCSC Ensembl
Outerchr7:4653295..4664117hg38UCSC Ensembl
chr7:4693926..4702748hg19UCSC Ensembl
Innerchr7:4694426..4702248hg19UCSC Ensembl
Outerchr7:4692926..4703748hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg388823
hg198823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1248e214
Supporting Variantsessv12671514, essv12671513
SamplesHG02614, HG03025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611943
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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