A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4019675



Internal ID22081306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144207186..144377836hg38UCSC Ensembl
Outerchr7:144199159..144378425hg38UCSC Ensembl
Innerchr7:143904279..144074929hg19UCSC Ensembl
Outerchr7:143896252..144075518hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38179267
hg19179267
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156752
Supporting Variants
Samples
Known GenesARHGEF34P, ARHGEF5, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4019675
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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