A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15976



Internal ID15835714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97924755..97930820hg38UCSC Ensembl
Outerchr7:97924279..97932097hg38UCSC Ensembl
Innerchr7:97554067..97560132hg19UCSC Ensembl
Outerchr7:97553591..97561409hg19UCSC Ensembl
Innerchr7:97392003..97398068hg18UCSC Ensembl
Outerchr7:97391527..97399345hg18UCSC Ensembl
Innerchr7:97198718..97204783hg17UCSC Ensembl
Outerchr7:97198242..97206060hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg387819
hg197819
hg187819
hg177819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8179
Supporting Variants
SamplesNA18552
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)nssv15976
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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