A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022226



Internal ID22083857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119180429..119287245hg38UCSC Ensembl
Outerchr7:119179596..119290452hg38UCSC Ensembl
Innerchr7:118820483..118927299hg19UCSC Ensembl
Outerchr7:118819650..118930506hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38110857
hg19110857
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156720
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022226
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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