A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891100



Internal ID19185496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40154661..40215523hg38UCSC Ensembl
Outerchr7:40153936..40225911hg38UCSC Ensembl
Innerchr7:40194260..40255122hg19UCSC Ensembl
Outerchr7:40193535..40265510hg19UCSC Ensembl
Innerchr7:40160785..40221647hg18UCSC Ensembl
Outerchr7:40160060..40232035hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3871976
hg1971976
hg1871976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781671, essv25779667, essv25797739, essv25780081
Samples
Known GenesC7orf10
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891100
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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