A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021105



Internal ID22082736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40373941..40466836hg38UCSC Ensembl
Outerchr7:40373714..40472863hg38UCSC Ensembl
Innerchr7:40413540..40506435hg19UCSC Ensembl
Outerchr7:40413313..40512462hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3899150
hg1999150
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156659
Supporting Variants
Samples
Known GenesC7orf10
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021105
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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