A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156748



Internal ID22087149
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv272n97
Supporting Variantsnssv4019669, nssv4019667, nssv4019666, nssv4019668
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)nsv1156748
Frequency
Sample Size131
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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