A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1672493



Internal ID15183315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7368356..7544523hg38UCSC Ensembl
Innerchr4:7370083..7546250hg19UCSC Ensembl
Innerchr4:7420984..7597150hg18UCSC Ensembl
Innerchr4:7434625..7610791hg16UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38176168
hg19176168
hg18176167
hg16176167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469758
Supporting Variants
Samples
Known GenesMIR4274, PSAPL1, SORCS2
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)nssv1672493
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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