A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749



Internal ID15843273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19579669..19588512hg38UCSC Ensembl
Outerchr7:19579223..19642798hg38UCSC Ensembl
Innerchr7:19619292..19628135hg19UCSC Ensembl
Outerchr7:19618846..19682421hg19UCSC Ensembl
Innerchr7:19585817..19594660hg18UCSC Ensembl
Outerchr7:19585371..19648946hg18UCSC Ensembl
Innerchr7:19392532..19401375hg17UCSC Ensembl
Outerchr7:19392086..19455661hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3863576
hg1963576
hg1863576
hg1763576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8068
Supporting Variants
SamplesNA19173
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)nssv15749
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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