A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16006



Internal ID15835711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:98025092..98027366hg38UCSC Ensembl
Outerchr7:98023605..98028623hg38UCSC Ensembl
Innerchr7:97654404..97656678hg19UCSC Ensembl
Outerchr7:97652917..97657935hg19UCSC Ensembl
Innerchr7:97492340..97494614hg18UCSC Ensembl
Outerchr7:97490853..97495871hg18UCSC Ensembl
Innerchr7:97299055..97301329hg17UCSC Ensembl
Outerchr7:97297568..97302586hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg385019
hg195019
hg185019
hg175019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8181
Supporting Variants
SamplesNA18552
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv16006
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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