A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15809



Internal ID15496550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37836886..37842657hg38UCSC Ensembl
Outerchr7:37833384..37906765hg38UCSC Ensembl
Innerchr7:37876488..37882259hg19UCSC Ensembl
Outerchr7:37872986..37946367hg19UCSC Ensembl
Innerchr7:37843013..37848784hg18UCSC Ensembl
Outerchr7:37839511..37912892hg18UCSC Ensembl
Innerchr7:37649728..37655499hg17UCSC Ensembl
Outerchr7:37646226..37719607hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3873382
hg1973382
hg1873382
hg1773382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8074
Supporting Variants
SamplesNA19173
Known GenesNME8, SFRP4
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)nssv15809
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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