A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614127



Internal ID7001022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91703858..91704765hg38UCSC Ensembl
Innerchr7:91703951..91704661hg38UCSC Ensembl
Outerchr7:91703808..91704815hg38UCSC Ensembl
chr7:91333173..91334080hg19UCSC Ensembl
Innerchr7:91333266..91333976hg19UCSC Ensembl
Outerchr7:91333123..91334130hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12889032, essv12889037, essv12889036, essv12889033, essv12889035, essv12889038, essv12889039, essv12889034
SamplesNA19332, NA19904, HG03380, NA19913, NA18907, NA19160, NA19380, HG02284
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614127
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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