A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779667



Internal ID19168338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40153936..40225911hg38UCSC Ensembl
Innerchr7:40193535..40265510hg19UCSC Ensembl
Innerchr7:40160060..40232035hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3871976
hg1971976
hg1871976
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891100
Supporting Variants
Samples
Known GenesC7orf10
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779667
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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