A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14987



Internal ID15836166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16309567..16365301hg38UCSC Ensembl
Outerchr7:16308894..16365670hg38UCSC Ensembl
Innerchr7:16349192..16404926hg19UCSC Ensembl
Outerchr7:16348519..16405295hg19UCSC Ensembl
Innerchr7:16315717..16371451hg18UCSC Ensembl
Outerchr7:16315044..16371820hg18UCSC Ensembl
Innerchr7:16122432..16178166hg17UCSC Ensembl
Outerchr7:16121759..16178535hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3856777
hg1956777
hg1856777
hg1756777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8061
Supporting Variants
SamplesNA18563
Known GenesISPD
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)nssv14987
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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