A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3672458



Internal ID18624053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144199147..144409403hg38UCSC Ensembl
Innerchr7:143896240..144106496hg19UCSC Ensembl
Innerchr7:143527173..143737429hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38210257
hg19210257
hg18210257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016605
Supporting Variants
Samples
Known GenesARHGEF34P, ARHGEF5, CTAGE4, CTAGE8, NOBOX, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3672458
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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