A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156712



Internal ID22087113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110551012..110576214hg38UCSC Ensembl
Outerchr7:110540711..110584548hg38UCSC Ensembl
Innerchr7:110191069..110216271hg19UCSC Ensembl
Outerchr7:110180768..110224605hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3843838
hg1943838
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022217
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156712
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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