A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15656



Internal ID15494789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:100271318..100272226hg38UCSC Ensembl
Outerchr7:100270859..100282158hg38UCSC Ensembl
Innerchr7:99868941..99869849hg19UCSC Ensembl
Outerchr7:99868482..99879781hg19UCSC Ensembl
Innerchr7:99706877..99707785hg18UCSC Ensembl
Outerchr7:99706418..99717717hg18UCSC Ensembl
Innerchr7:99513592..99514500hg17UCSC Ensembl
Outerchr7:99513133..99524432hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3811300
hg1911300
hg1811300
hg1711300
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8182
Supporting Variants
SamplesNA19007
Known GenesGATS
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)nssv15656
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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