A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021106



Internal ID22082737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40914664..40948290hg38UCSC Ensembl
Outerchr7:40912809..40964726hg38UCSC Ensembl
Innerchr7:40954263..40987889hg19UCSC Ensembl
Outerchr7:40952408..41004325hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3851918
hg1951918
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156660
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021106
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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