A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4019591



Internal ID22081222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143525988..143835905hg38UCSC Ensembl
Outerchr7:143521875..143846758hg38UCSC Ensembl
Innerchr7:143223081..143532998hg19UCSC Ensembl
Outerchr7:143218968..143543851hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38324884
hg19324884
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156740
Supporting Variants
Samples
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115C, LOC154761
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4019591
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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