A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4019669



Internal ID22081300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144199159..144354138hg38UCSC Ensembl
Outerchr7:144176859..144369854hg38UCSC Ensembl
Innerchr7:143896252..144051231hg19UCSC Ensembl
Outerchr7:143873952..144066947hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38192996
hg19192996
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156748
Supporting Variants
Samples
Known GenesARHGEF34P, ARHGEF35, 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)nssv4019669
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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