A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891101



Internal ID18838811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40263685..40311288hg38UCSC Ensembl
Outerchr7:40263685..40320658hg38UCSC Ensembl
Innerchr7:40303284..40350887hg19UCSC Ensembl
Outerchr7:40303284..40360257hg19UCSC Ensembl
Innerchr7:40269809..40317412hg18UCSC Ensembl
Outerchr7:40269809..40326782hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3856974
hg1956974
hg1856974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781737, essv25799961
Samples
Known GenesC7orf10
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891101
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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