A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3019669



Internal ID15214865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122053329..122053329hg38UCSC Ensembl
chr12:122491235..122491235hg19UCSC Ensembl
chr12:120975618..120975618hg18UCSC Ensembl
chr12:120953955..120953955hg17UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381
hg191
hg181
hg171
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv473912
Supporting Variants
SamplesNA12156
Known GenesBCL7A
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)nssv3019669
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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