A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156752



Internal ID22087153
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv272n97
Supporting Variantsnssv4019675
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)nsv1156752
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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