A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4019665



Internal ID22081296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144199159..144336758hg38UCSC Ensembl
Outerchr7:144176859..144343824hg38UCSC Ensembl
Innerchr7:143896252..144033851hg19UCSC Ensembl
Outerchr7:143873952..144040917hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38166966
hg19166966
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156747
Supporting Variants
Samples
Known GenesARHGEF34P, ARHGEF35, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4019665
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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