A curated catalogue of human genomic structural variation

Variant Details

Variant: nsv471092

Internal ID15210965
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:67174030..67518392hg38UCSC Ensembl
Innerchr16:67207933..67552295hg19UCSC Ensembl
Innerchr16:65765434..66109796hg18UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv545330
Known GenesAGRP, ATP6V0D1, E2F4, ELMO3, EXOC3L1, FHOD1, HSD11B2, KCTD19, KIAA0895L, LOC100505942, LRRC29, LRRC36, MIR328, NOL3, PLEKHG4, SLC9A5, TMEM208, TPPP3, ZDHHC1
MethodSNP array
AnalysisWe used the previously validated default quality control criteria, excluding samples with a log R ratio standard deviation of >0.28, a median B allele frequency of >0.55 or <0.45, or a B allele frequency drift of >0.002 (for more details see Wang et al. 2007). As the PennCNV algorithm is more sensitive and specific to CNVs covering greater numbers of SNPs in the HumanHap550 array, use of a minimum number of SNPs in CNV detection increases the reliability of CNV calls (with a consequent reduction in calls per individual). We set 10 SNPs as the minimum detection threshold in the algorithm.
PlatformIllumina HumanHap550 Genotyping BeadChip v3
CommentsSingle-copy duplication
Pubmed ID18288195
Accession Number(s)nsv471092
Sample Size443
Observed Gain1
Observed Loss0
Observed Complex0

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