A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15714



Internal ID15493423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150150939..150151480hg38UCSC Ensembl
Outerchr7:150150444..150151609hg38UCSC Ensembl
Innerchr7:149848028..149848569hg19UCSC Ensembl
Outerchr7:149847533..149848698hg19UCSC Ensembl
Innerchr7:149478961..149479502hg18UCSC Ensembl
Outerchr7:149478466..149479631hg18UCSC Ensembl
Innerchr7:149285676..149286217hg17UCSC Ensembl
Outerchr7:149285181..149286346hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg381166
hg191166
hg181166
hg171166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8229
Supporting Variants
SamplesNA18975
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)nssv15714
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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