A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1673722



Internal ID15184544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35855717..36039894hg38UCSC Ensembl
Innerchr7:35895327..36079504hg19UCSC Ensembl
Innerchr7:35861852..36046029hg18UCSC Ensembl
Innerchr7:35636531..35820718hg16UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38184178
hg19184178
hg18184178
hg16184188
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469590
Supporting Variants
Samples
Known GenesSEPT7
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nssv1673722
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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