A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv473631



Internal ID15226379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130506625..130506625hg38UCSC Ensembl
chr7:130146466..130146466hg19UCSC Ensembl
chr7:129933702..129933702hg18UCSC Ensembl
chr7:129740417..129740417hg17UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg381
hg191
hg181
hg171
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3017868
SamplesNA19129
Known GenesCOPG2
MethodSequencing
AnalysisSearch fosmid ESPs as described in Tuzun et al (2005)
PlatformAgilent Custom Human 244K CGH Array
CommentsOEA singleton. The coordinate provided is from the mappable member of a fosmid end sequence pair, and indicates the genomic vicinity of a novel sequence insertion
ReferenceKidd_et_al_2010
Pubmed ID20440878
Accession Number(s)nsv473631
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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